DNA replication ATP-dependent helicase/nuclease DNA2 isoform h4 (human)


1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-4 isoform h4 (human)


cyclic AMP-responsive element-binding protein 3 isoform h2 (human)


phosphatidylinositol transfer protein beta isoform, initiator methionine removed form (human)


protein VAC14 homolog isoform h2 (human)


neuropeptide FF receptor 2 isoform h2 (human)


inactive rhomboid protein 1 isoform m1 (mouse)


elongation factor Ts, mitochondrial isoform h3 (human)


chromodomain-helicase-DNA-binding protein 1-like isoform h2 (human)


heparan-sulfate 6-O-sulfotransferase 1 isoform h2 (human)


beta-galactoside alpha-2,6-sialyltransferase 1 isoform h2 (human)


carnitine O-acetyltransferase N-glycosylated 1 (human)


5'-3' exonuclease PLD3 N-glycosylated 1 (human)


aggrecan core protein O-glycosylated 62 (human)


plasminogen activator inhibitor 1 N-glycosylated 2 (human)


GPI mannosyltransferase 1 isoform 1 (human)


C-C motif chemokine 16, signal peptide removed form (human)


protein kinase C theta type phosphorylated 3 (human)


tropomyosin alpha-3 chain isoform h7 (human)


bone morphogenetic protein 2 isoform 1 (human)


ATP-binding cassette sub-family C member 5 isoform h2 (human)


1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3


serine/threonine-protein kinase Nek9, initiator methionine removed phosphorylated 4 (human)


helicase POLQ-like N-glycosylated 1 (human)


glutathione S-transferase A2, initiator methionine removed form (human)


putative ATP-dependent RNA helicase DDX11-like protein 8


iron-sulfur cluster assembly 2, mitochondrial


LLGL scribble cell polarity complex component 2 isoform A (human)


cyclin-dependent kinase 10 isoform h5 (human)


serine/threonine-protein kinase 4 phosphorylated 1 (human)


voltage-gated potassium channel subunit beta-2 isoform h4 (human)


mothers against decapentaplegic homolog 3 isoform h4 (human)


inositol 1,4,5-triphosphate receptor associated 1 isoform h2 (human)


beta-glucuronidase, signal peptide removed form (human)


isoaspartyl peptidase/L-asparaginase isoform h1 (human)


pyridine nucleotide-disulfide oxidoreductase domain-containing protein 1 isoform h2 (human)


protocadherin gamma-A2 isoform h1 (human)


inositol 1,4,5-trisphosphate receptor type 2


endoplasmic reticulum aminopeptidase 1 isoform h2 (human)


ectonucleoside triphosphate diphosphohydrolase 4


retinal dehydrogenase 2 isoform 1 (human)


mitochondrial ornithine transporter 1 isoform 1 (human)


protein kinase C theta type phosphorylated 1 (human)


histone H2A type 1-B/E, initiator methionine removed dimethylated 1 (human)


sterol O-acyltransferase 1 isoform h1 (human)


versican core protein O-glycosylated 227 (human)


2-amino-3-ketobutyrate coenzyme A ligase


latent-transforming growth factor beta-binding protein 4 O-glycosylated 13 (human)


voltage-dependent L-type calcium channel subunit beta-2 isoform h2h (human)


peroxisome proliferator-activated receptor delta isoform h2 (human)


diacylglycerol kinase epsilon isoform h1 (human)


2-aminomuconic semialdehyde dehydrogenase isoform 1 (human)


17-beta-hydroxysteroid dehydrogenase type 3 isoform h2 (human)


solute carrier family 4 member 11 isoform h3 (human)


N-acetyllactosaminide beta-1,6-N-acetylglucosaminyl-transferase isoform B (human)


ectonucleoside triphosphate diphosphohydrolase 3


pyridoxal phosphate phosphatase PHOSPHO2


serine/threonine-protein kinase VRK2 isoform h2 (human)


serine/threonine-protein kinase haspin unphosphorylated form (human)


sterol regulatory element-binding protein cleavage-activating protein isoform h1 (human)


S-acyl fatty acid synthase thioesterase, medium chain isoform h2 (human)


glutamate receptor 1, signal peptide removed form (human)


coagulation factor XIII A chain isoform 1 (human)


ubiquitin carboxyl-terminal hydrolase 2 isoform h3 (human)


NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9 isoform 1 (human)


crossover junction endonuclease EME1 isoform h1 (human)


ornithine aminotransferase, mitochondrial isoform h2 (human)


galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 1 isoform 1 (human)


kynurenine formamidase isoform h2 (human)


protein phosphatase 2C-like domain-containing protein 1 isoform h2 (human)


peptidyl-tRNA hydrolase 2, mitochondrial, transit peptide removed form (human)


aminoacyl tRNA synthase complex-interacting multifunctional protein 1 isoform h2 (human)


lysine-specific demethylase 2B isoform h5 (human)


GPI transamidase component PIG-S, initiator methionine removed form (human)


thiamin pyrophosphokinase 1 isoform 1 (human)


3 beta-hydroxysteroid dehydrogenase type 7 isoform h2 (human)


5'-nucleotidase domain-containing protein 3 isoform h1 (human)


zinc-alpha-2-glycoprotein N-glycosylated 10 (human)


serine/threonine-protein kinase Nek10 isoform h5 (human)


immunoglobulin heavy constant mu N-glycosylated 122 (human)


Kv channel-interacting protein 2 isoform 4 (human)


ubiquitin carboxyl-terminal hydrolase 40


BDNF/NT-3 growth factors receptor, signal peptide removed form (human)


dynamin-1-like protein isoform h2 (human)


2-hydroxyacyl-CoA lyase 1 isoform h1 (human)


mitochondrial 2-oxoglutarate/malate carrier protein isoform h2 (human)


phosphoserine aminotransferase isoform h2 (human)


receptor-type tyrosine-protein phosphatase H isoform h2 (human)


very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 1


neutral alpha-glucosidase AB isoform 2 (human)


glycerol-3-phosphate dehydrogenase, mitochondrial, transit peptide removed form (human)


organic solute transporter subunit alpha isoform 1 (mouse)


signal recognition particle 54 kDa protein isoform 1 (human)


ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1 N-glycosylated 3 (rat)


m7GpppN-mRNA hydrolase isoform h2 (human)


synaptic vesicular amine transporter isoform h2 (human)


apoptotic protease-activating factor 1 isoform 3 (human)


leukocyte-associated immunoglobulin-like receptor 1 isoform h2 (human)


ephrin type-A receptor 8, signal peptide removed form (human)


neuronal acetylcholine receptor subunit beta-4 isoform h2 (human)


cyclic nucleotide-gated cation channel beta-1 isoform hRCNC2A (human)


ATP synthase-coupling factor 6, mitochondrial


angiotensinogen N-glycosylated 3 (human)


cyclic AMP-dependent transcription factor ATF-2 isoform h6 (human)


acyl-CoA-binding domain-containing protein 5 isoform h2 (human)


T-cell surface glycoprotein CD1e, membrane-associated isoform h1 (human)


3-ketodihydrosphingosine reductase isoform 1 (human)


chymotrypsin-like elastase family member 3B N-glycosylated 21 (human)


myotonin-protein kinase isoform h9 (human)


coatomer subunit beta' isoform h1 (human)


citron Rho-interacting kinase isoform h1 (human)


versican core protein O-glycosylated 97 (human)


electrogenic sodium bicarbonate cotransporter 1


N-terminal acetyltransferase complex ARD1 subunit B


basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 16 (human)


immunoglobulin heavy constant mu N-glycosylated 137 (human)


long-chain fatty acid transport protein 2 isoform 1 (human)


versican core protein O-glycosylated 265 (human)


calmodulin-lysine N-methyltransferase isoform 1 (human)


tRNA (guanine(10)-N2)-methyltransferase homolog isoform h3 (human)


aspartate dehydrogenase domain-containing protein isoform h1 (human)


dehydrogenase/reductase SDR family member 4 isoform h4 (human)


inactive tyrosine-protein kinase 7 N-glycosylated 4 (human)


phospholipid phosphatase 4 isoform h4 (human)


cholinephosphotransferase 1 isoform h1 (human)


aminomethyltransferase, mitochondrial isoform 1 (human)


peptidoglycan recognition protein 4 isoform h2 (human)


sodium- and chloride-dependent GABA transporter 1 isoform 1 (human)


copper-transporting ATPase 2 isoform h5 (human)


deleted in malignant brain tumors 1 protein isoform h2 (human)


glutamate--cysteine ligase regulatory subunit isoform 1 (human)


maternal embryonic leucine zipper kinase


amine oxidase [flavin-containing] B, initiator methionine removed form (human)


versican core protein O-glycosylated 242 (human)


sodium-coupled monocarboxylate transporter 2 isoform h2 (human)


BDNF/NT-3 growth factors receptor isoform h5 (human)


potassium voltage-gated channel subfamily H member 6 isoform 1 (human)


carbonyl reductase [NADPH] 3 isoform 1 (human)


prostatic acid phosphatase N-glycosylated 1 (human)


phospholipid-transporting ATPase VD isoform h1 (human)


glyceraldehyde-3-phosphate dehydrogenase phosphorylated 1 (human)


voltage-gated hydrogen channel 1 isoform h2 (human)


gamma-aminobutyric acid receptor subunit alpha-5, signal peptide removed form (human)


galactosylceramide sulfotransferase O-glycosylated 2 (human)


carbohydrate sulfotransferase 5 isoform h2 (human)


45 kDa calcium-binding protein isoform h1 (human)


DNA repair protein complementing XP-A cells


sodium/potassium-transporting ATPase subunit alpha-3


multiple C2 and transmembrane domain-containing protein 2 isoform h5 (human)


tyrosine-protein kinase JAK2 isoform 1 phosphorylated 1 (human)


reduced folate transporter isoform h3 (human)


cartilage oligomeric matrix protein isoform h2 (human)


versican core protein O-glycosylated 269 (human)


follistatin-related protein 3 isoform 1 (mouse)


voltage-dependent L-type calcium channel subunit alpha-1C isoform h28 (human)


methyl-CpG-binding domain protein 1 isoform h5 (human)


transient receptor potential cation channel subfamily M member 8 isoform 2 (human)


phosphorylase b kinase gamma catalytic chain, skeletal muscle/heart isoform isoform 1 (human)


collagen alpha-1(XVIII) chain O-glycosylated 26 (human)


apolipoprotein B-100 N-glycosylated 3 (human)


mitochondrial tRNA methylthiotransferase CDK5RAP1


heme oxygenase 2, initiator methionine removed form (human)


peptidyl-prolyl cis-trans isomerase FKBP5 isoform h2 (human)


dihydropyrimidine dehydrogenase [NADP(+)] isoform h2 (human)


Ran-binding protein 3 isoform h1 (human)


versican core protein O-glycosylated 180 (human)


Rho guanine nucleotide exchange factor 40


fidgetin-like protein 1 isoform h2 (human)


dimethylglycine dehydrogenase, mitochondrial isoform h2 (human)


tubulin beta-4B chain phosphorylated 1 (human)


receptor-type tyrosine-protein phosphatase U isoform 1 (human)


cyclin-dependent kinase 2 isoform h2 (human)


phospholipid phosphatase-related protein type 5 isoform 2 (human)


mitochondrial sodium/calcium exchanger protein


dolichyl-diphosphooligosaccharide--protein glycosyltransferase 48 kDa subunit isoform h2 (human)


NADH dehydrogenase [ubiquinone] iron-sulfur protein 5, initiator methionine removed form (human)


voltage-gated potassium channel subunit KCNQ1 sequence variant F339del (human)


peptidyl-prolyl cis-trans isomerase A, initiator methionine removed form (human)


phosphatidylinositol-glycan-specific phospholipase D N-glycosylated 2 (human)


serine/threonine-protein kinase receptor R3 sequence variant R479L (human)


amyloid-beta precursor protein O-glycosylated 7 (human)


gamma-aminobutyric acid receptor subunit beta-2 isoform h4 (human)


Ral guanine nucleotide dissociation stimulator-like 2


serine/threonine-protein kinase greatwall isoform h1 (human)


long-chain-fatty-acid--CoA ligase ACSBG2 isoform h3 (human)


receptor activity-modifying protein 1 isoform 1 (human)


V-type proton ATPase 116 kDa subunit a 2


aspartyl/asparaginyl beta-hydroxylase isoform h8 (human)


NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial, transit peptide removed form (human)


vitamin K-dependent protein C N-glycosylated 11 (human)


structure-specific endonuclease subunit SLX1


NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 6 isoform 1 (human)


tRNA (cytosine(38)-C(5))-methyltransferase isoform C (human)


troponin T, fast skeletal muscle isoform h3 (human)


E3 ubiquitin-protein ligase Mdm2 N-glycosylated 1 (human)


high affinity nerve growth factor receptor isoform TrkA-I mature form N-glycosylated and phosphorylated 1 (human)


myosin light chain 1/3, skeletal muscle isoform


cyclin-G-associated kinase isoform h2 (human)


sialic acid-binding Ig-like lectin 7 isoform h4 (human)


Rab9 effector protein with kelch motifs phosphoserine form (human)


syndecan-2, signal peptide removed form (human)


latent-transforming growth factor beta-binding protein 3 O-glycosylated 1 (human)


cytochrome c oxidase subunit 5B, mitochondrial, transit peptide removed form (human)


peroxisomal N(1)-acetyl-spermine/spermidine oxidase isoform h4 (human)


inhibitor of growth protein 4 isoform h5 (human)


triggering receptor expressed on myeloid cells 2 isoform h2 sequence variant E202D (human)


NAD-dependent protein deacylase sirtuin-6 isoform h2 (human)


leukocyte immunoglobulin-like receptor subfamily B member 4, signal peptide removed form (human)


T-cell surface glycoprotein CD1e, membrane-associated isoform h11 (human)


probable cation-transporting ATPase 13A4 isoform h3 (human)


serine/threonine-protein kinase PINK1, mitochondrial, transit peptide removed form (human)


heparan sulfate glucosamine 3-O-sulfotransferase 1, signal peptide removed form (human)


Rho guanine nucleotide exchange factor TIAM2 isoform h5 (human)


bifunctional heparan sulfate N-deacetylase/N-sulfotransferase 3 isoform h2 (human)


transcriptional activator GLI3 phosphorylated form (human)


mitogen-activated protein kinase kinase kinase kinase 2 isoform h2 (human)


guanine nucleotide-binding protein G(s) subunit alpha isoform XLas-3 (human)


RAS guanyl-releasing protein 1 isoform h4 (human)


matrix metalloproteinase-16 isoform Long (human)


NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 11, mitochondrial isoform h1 (human)


pleckstrin homology domain-containing family M member 3 isoform h1 (human)


electrogenic sodium bicarbonate cotransporter 4 isoform h4 (human)


medium-chain acyl-CoA ligase ACSF2, mitochondrial, transit peptide removed form (human)


RAC-beta serine/threonine-protein kinase phosphorylated 2 (human)


immunoglobulin heavy constant mu N-glycosylated 2 (human)


GTP-binding protein 1 O-glycosylated 2 (human)


delta-type opioid receptor isoform 1 (human)


mitogen-activated protein kinase kinase kinase 1


receptor-interacting serine/threonine-protein kinase 2 ubiquitinated 1 (human)


TBC1 domain family member 23 isoform h1 (human)


disrupted in schizophrenia 1 protein isoform h6 (human)


tropomyosin alpha-1 chain isoform 1 (human)


solute carrier family 12 member 1 isoform A (human)


solute carrier family 7 member 13 isoform h1 (human)


phosphatidylinositol 4,5-bisphosphate 5-phosphatase A


histone acetyltransferase KAT6B isoform h2 (human)


aggrecan core protein O-glycosylated 24 (human)


transient receptor potential cation channel subfamily V member 4 isoform C (human)


pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial isoform h2 (human)


aggrecan core protein O-glycosylated 94 (human)


serine/threonine-protein kinase N2 isoform h3 (human)


fatty acid hydroxylase domain-containing protein 2


choline/ethanolamine kinase, initiator methionine removed form (human)


voltage-gated potassium channel subunit KCNQ3


phosphatidylinositol 4-phosphate 5-kinase type-1 beta


GPI ethanolamine phosphate transferase 1


tissue-type plasminogen activator N-glycosylated 1 (human)


solute carrier organic anion transporter family member 1C1 isoform h4 (human)


alpha-1,3/1,6-mannosyltransferase ALG2 isoform h2 (human)


ephrin type-A receptor 5 isoform h3 (human)


neutral and basic amino acid transport protein rBAT isoform D (human)


dual specificity protein phosphatase 1 acetylated 1 (human)


palmitoyltransferase ZDHHC20 isoform h3 (human)


potassium channel subfamily T member 1 isoform h4 (human)


prolyl hydroxylase EGLN3 isoform 1 (human)


1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase epsilon-1 isoform h1 (human)


cGMP-specific 3',5'-cyclic phosphodiesterase isoform hPDE5A1 (human)


high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8A isoform h1 (human)


receptor-type tyrosine-protein phosphatase C isoform CD45RB (human)


serine/threonine-protein phosphatase PP1-beta catalytic subunit


amine oxidase [flavin-containing] B isoform h2 (human)


epidermal growth factor receptor N-glycosylated 10 (human)


versican core protein O-glycosylated 64 (human)


glutamate receptor ionotropic, kainate 1 isoform h1 (human)


immunoglobulin heavy constant mu N-glycosylated 116 (human)


glutathione hydrolase 5 proenzyme O-glycosylated 5 (human)


putative sodium-coupled neutral amino acid transporter 8


histone-lysine N-methyltransferase SETDB2 isoform h1 (human)


cyclic GMP-AMP synthase isoform h1 (human)


ubiquitin carboxyl-terminal hydrolase 15 isoform 2 (human)


retinoic acid receptor RXR-alpha phosphorylated 1 (human)


72 kDa type IV collagenase, signal peptide removed form (human)


GTPase IMAP family member 5 isoform h2 (human)


Rho guanine nucleotide exchange factor 7 isoform h5 (human)


retinal dehydrogenase 2 isoform h2 (human)


translocon-associated protein subunit gamma


metabotropic glutamate receptor 5 isoform h1 (human)


pyridoxine-5'-phosphate oxidase isoform h2 (human)


TGF-beta 1 sequence variant C225R (human)


poly [ADP-ribose] polymerase tankyrase-1 isoform h1 (human)


prostaglandin-H2 D-isomerase N-glycosylated 13 (human)


sodium-coupled monocarboxylate transporter 1


adhesion G protein-coupled receptor L2 isoform h1 (human)


serine/threonine-protein kinase receptor R3 sequence variant R411P (human)


hepatoma-derived growth factor isoform h3 (human)


protein tyrosine phosphatase domain-containing protein 1 isoform h1 (human)


serine/threonine-protein kinase receptor R3 sequence variant R411Q (human)


protein arginine N-methyltransferase 1 isoform V2 (human)


interleukin-1 receptor-associated kinase 4 unmodified form (human)


alkaline phosphatase, tissue-nonspecific isozyme, mature form (human)


peroxisomal multifunctional enzyme type 2 isoform h2 (human)


latent-transforming growth factor beta-binding protein 4 isoform h3 (human)


pseudouridylate synthase PUS7L isoform h1 (human)


dual specificity mitogen-activated protein kinase kinase 3


Rho GTPase-activating protein 9 isoform h4 (human)


aggrecan core protein O-glycosylated 105 (human)


Ras association domain-containing protein 1 isoform F (human)


cytochrome b5, initiator methionine removed form (human)


RNA-binding protein EWS isoform h4 (human)


prenylcysteine oxidase 1 N-glycosylated 3 (human)


membrane-associated progesterone receptor component 2 isoform h1 (human)


protein kinase C iota type, initiator methionine removed form (human)


hereditary hemochromatosis protein isoform h5 (human)


NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 3 isoform 1 (human)


receptor tyrosine-protein kinase erbB-2, signal peptide removed phosphorylated 3 (human)


mitogen-activated protein kinase kinase kinase kinase 1 isoform h2 (human)


serine--tRNA ligase, mitochondrial isoform 1 (human)


histidine-rich glycoprotein O-glycosylated 4 (human)


major prion protein N-glycosylated 1 (human)


heparin cofactor 2 O-glycosylated 11 (human)


voltage-dependent calcium channel subunit alpha-2/delta-4 isoform h5 (human)


calcium-dependent secretion activator 1 isoform h4 (human)


epithelial discoidin domain-containing receptor 1, signal peptide removed form (human)


immunoglobulin heavy constant mu N-glycosylated 82 (human)


ATP-binding cassette sub-family C member 6 isoform h3 (human)


ADP-dependent glucokinase isoform h5 (human)


alcohol dehydrogenase 6 isoform h2 (human)


1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase zeta-1 isoform h1 (human)


superoxide dismutase [Mn], mitochondrial isoform h4 (human)


cell division cycle-associated 7-like protein isoform h4 (human)


NADH-cytochrome b5 reductase-like isoform h3 (human)


dual specificity tyrosine-phosphorylation-regulated kinase 3 isoform h2 (human)


prolyl endopeptidase FAP isoform h1 (human)


aggrecan core protein O-glycosylated 64 (human)


receptor-type tyrosine-protein phosphatase eta isoform h3 (human)


collagen alpha-1(XIII) chain isoform h6 (human)


sarcoplasmic/endoplasmic reticulum calcium ATPase 3


transient receptor potential cation channel TRPA1


low-density lipoprotein receptor isoform h1 (human)


translocon-associated protein subunit alpha N-glycosylated 4 (human)


nuclear receptor coactivator 3 isoform 1 acetylated 1 (human)


E3 ubiquitin-protein ligase UBR2 isoform 4 (human)


iron-sulfur cluster assembly 1 homolog, mitochondrial isoform h2 (human)


acetyl-CoA carboxylase 2 isoform h1 (human)


phosphatidylserine synthase 1 isoform 1 (human)


phosphatidylinositol 3,4,5-trisphosphate-dependent Rac exchanger 2 protein N-glycosylated 1 (human)


testis-specific serine/threonine-protein kinase 4


tricarboxylate transport protein, mitochondrial


interstitial collagenase N-glycosylated 20 (human)


1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma-1, initiator methionine removed form (human)


glutaminase kidney isoform, mitochondrial isoform h1 (human)


methylglutaconyl-CoA hydratase, mitochondrial isoform h1 (human)


epidermal growth factor receptor N-glycosylated 2 (human)


immunoglobulin heavy constant mu N-glycosylated 102 (human)


angiotensin-converting enzyme isoform hSomatic-1 (human)


ubiquitin carboxyl-terminal hydrolase 10, initiator methionine removed form (human)


tyrosine-protein kinase ABL2 isoform h2 (human)


TGF-beta receptor type-2 sequence variant T315M (human)


ubiquitin-conjugating enzyme E2 N isoform 1 (human)


NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 1 isoform 1 (human)


cytochrome c oxidase subunit 5B, mitochondrial


C-X-C chemokine receptor type 4 isoform mCXCR4-B (mouse)


aspartyl/asparaginyl beta-hydroxylase isoform h7 (human)


amiloride-sensitive sodium channel subunit gamma


ATPase family AAA domain-containing protein 2 isoform h1 (human)


protein phosphatase methylesterase 1 isoform h4 (human)


palmitoyltransferase ZDHHC6 isoform 1 (human)


guanine nucleotide exchange factor VAV3 phosphorylated 1 (human)


T-cell surface glycoprotein CD1e, membrane-associated isoform h5 (human)


collagen alpha-1(XVIII) chain O-glycosylated 13 (human)


prostaglandin-H2 D-isomerase N-glycosylated 22 (human)


methyl-CpG-binding domain protein 1 isoform m5 (mouse)


heparan sulfate glucosamine 3-O-sulfotransferase 3A1


versican core protein O-glycosylated 43 (human)


neuroendocrine convertase 2 isoform h1 (human)


cAMP-dependent protein kinase catalytic subunit beta isoform h9 (human)


dual specificity protein phosphatase 13 isoform 5 (human)


Rap guanine nucleotide exchange factor 6 isoform h5 (human)


calcium-transporting ATPase type 2C member 2 isoform h3 (human)


short transient receptor potential channel 7 isoform 1 (human)


protocadherin gamma-A7 isoform h1 (human)


phosphorylase b kinase gamma catalytic chain, liver/testis isoform


CMP-N-acetylneuraminate-beta-1,4-galactoside alpha-2,3-sialyltransferase isoform hB1+32 (human)


phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN


propionyl-CoA carboxylase beta chain, mitochondrial, transit peptide removed form (human)


nuclear factor of activated T-cells, cytoplasmic 4 isoform h1 (human)


ephrin type-B receptor 6 isoform h3 (human)


membrane-bound transcription factor site-1 protease


alpha-fetoprotein N-glycosylated 10 (human)


PI-PLC X domain-containing protein 2 isoform h2 (human)


protein unc-13 homolog B isoform h2 (human)


aurora kinase B unphosphorylated form (human)


aconitate hydratase, mitochondrial, transit peptide removed form (human)


mineralocorticoid receptor isoform h1 (human)


aggrecan core protein O-glycosylated 16 (human)


mitogen-activated protein kinase 12 isoform h2 (human)


ubiquitin-protein ligase E3A isoform II (human)


aminopeptidase N O-glycosylated 4 (human)


formimidoyltransferase-cyclodeaminase isoform C (human)


cytosolic phospholipase A2 delta isoform h2 (human)


sterol O-acyltransferase 2 isoform h1 (human)


prostaglandin E synthase 3 isoform h2 (human)


mannose-1-phosphate guanyltransferase alpha isoform h2 (human)


transmembrane protein 132A isoform h3 (human)


cyclic nucleotide-gated cation channel alpha-3 sequence variant R283Q (human)


DNA-directed RNA polymerases I, II, and III subunit RPABC3


iodotyrosine deiodinase 1 isoform h7 (human)


single-strand selective monofunctional uracil DNA glycosylase isoform h1 (human)


probable proline--tRNA ligase, mitochondrial


general transcription and DNA repair factor IIH helicase subunit XPD


phospholipid phosphatase-related protein type 3 isoform h1 (human)


pterin-4-alpha-carbinolamine dehydratase, initiator methionine removed form (human)


2-oxoglutarate dehydrogenase-like, mitochondrial isoform h1 (human)


2-oxoglutarate and iron-dependent oxygenase domain-containing protein 2 isoform h1 (human)


mitogen-activated protein kinase kinase kinase 20 isoform h1 (human)


phospholipid phosphatase 4 isoform h3 (human)


sodium bicarbonate cotransporter 3 isoform h10 (human)


latent-transforming growth factor beta-binding protein 1 O-glycosylated 11 (human)


vesicular glutamate transporter 1 isoform h3 (human)


chymotrypsin-like elastase family member 1


alpha-N-acetylgalactosaminidase N-glycosylated 63 (human)


SUMO-activating enzyme subunit 1 isoform h1 (human)


aggrecan core protein O-glycosylated 9 (human)


bone morphogenetic protein 2 isoform 1, mature form (human)


tissue-type plasminogen activator N-glycosylated 74 (human)


bifunctional methylenetetrahydrofolate dehydrogenase/cyclohydrolase, mitochondrial, transit peptide removed form (human)


sodium/glucose cotransporter 1 isoform h2 (human)


ATP-binding cassette sub-family C member 5


mitochondrial coenzyme A diphosphatase NUDT8 isoform h2 (human)


STE20-related kinase adapter protein alpha isoform h2 (human)


cannabinoid receptor 1 isoform h3 (human)


glial cell line-derived neurotrophic factor isoform h4 (human)


chromodomain-helicase-DNA-binding protein 2 isoform h1 (human)


tyrosine--tRNA ligase, cytoplasmic isoform 1 (human)


apolipoprotein D N-glycosylated 22 (human)


histidine decarboxylase isoform h2 (human)


phospholipid scramblase 2 isoform h3 (human)


chondroitin sulfate N-acetylgalactosaminyltransferase 1 O-glycosylated 1 (human)


phosphatidylinositol 3-kinase regulatory subunit alpha isoform h2 (human)


ATP synthase F(0) complex subunit B1, mitochondrial, transit peptide removed form (human)


calcium/calmodulin-dependent protein kinase type II subunit gamma isoform h9 (human)


telomerase reverse transcriptase isoform h4 (human)


E3 ubiquitin-protein ligase NEDD4-like isoform h6 (human)


protocadherin-11 X-linked isoform h8 (human)


sigma non-opioid intracellular receptor 1 isoform 1 (human)


immunoglobulin heavy constant mu N-glycosylated 15 (human)


scavenger receptor class B member 1 isoform h3 (human)


ectonucleoside triphosphate diphosphohydrolase 2 isoform gamma (human)


DNA-directed DNA/RNA polymerase mu isoform h2 (human)


general transcription factor 3C polypeptide 4


fibroblast growth factor 23, signal peptide removed form (human)


immunoglobulin heavy constant mu N-glycosylated 101 (human)


nuclear factor of activated T-cells, cytoplasmic 3 isoform h6 (human)


mRNA decay activator protein ZFP36 phosphorylated 1 (human)


hydroxymethylglutaryl-CoA lyase, mitochondrial isoform h3 (human)


lateral signaling target protein 2 homolog isoform h8 (human)


hematopoietic cell signal transducer, signal peptide removed form (human)


sodium- and chloride-dependent GABA transporter 3


transient receptor potential cation channel TRPM8


endothelin-converting enzyme 1 isoform D (human)


transcription factor PML isoform 3 (human)


cytosolic acyl coenzyme A thioester hydrolase


alpha-N-acetylgalactosaminidase N-glycosylated 99 (human)


cytosolic 5'-nucleotidase 3A isoform h4 (human)


branched-chain-amino-acid aminotransferase, cytosolic isoform h3 (human)


60 kDa lysophospholipase isoform h3 (human)


alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B isoform h2 (human)


putative bifunctional UDP-N-acetylglucosamine transferase and deubiquitinase ALG13 isoform h2 (human)


serum amyloid P-component O-glycosylated 1 (human)


alpha-2-macroglobulin N-glycosylated 17 (human)


voltage-gated potassium channel subunit KCNQ1 sequence variant T391I (human)


Rab3 GTPase-activating protein catalytic subunit isoform h1 (human)


2-hydroxyacylsphingosine 1-beta-galactosyltransferase, signal peptide removed form (human)


fibrinogen gamma chain N-glycosylated 2 (human)


homeobox protein Meis1 isoform h2 (human)


estradiol 17-beta-dehydrogenase 11, signal peptide removed form (human)


AP-2 complex subunit mu phosphorylated 1 (human)


dual specificity protein phosphatase 15 isoform h2 (human)


heparin cofactor 2 N-glycosylated 4 (human)


beta-alanine-activating enzyme isoform h1 (human)


mu-type opioid receptor isoform h11 (human)


importin subunit alpha-1 isoform 1 (human)


a disintegrin and metalloproteinase with thrombospondin motifs 2 isoform LpNPI (human)


lysosomal alpha-glucosidase N-glycosylated 1 (human)


sodium channel protein type 5 subunit alpha isoform h2 (human)


inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 1 isoform h2 (human)


glyceraldehyde-3-phosphate dehydrogenase isoform 1 (human)


NADH dehydrogenase [ubiquinone] flavoprotein 2, mitochondrial, transit peptide removed form (human)


1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma-2 phosphorylated 2 (human)


prolyl hydroxylase EGLN2 isoform hp40 (human)


vascular anomaly

biolink:Disease biolink:DiseaseOrPhenotypicFeature biolink:ThingWithTaxon biolink:BiologicalEntity biolink:NamedThing biolink:Entity


Metastatic Rectal Squamous Cell Carcinoma


Locally Advanced Rectal Squamous Cell Carcinoma


Stage IIIB Ovarian Germ Cell Tumor AJCC v6 and 7


Stage IIIA Ovarian Cancer AJCC v6 and v7


Recurrent Malignant Ovarian Brenner Tumor


Stage IC Ovarian Germ Cell Tumor AJCC v6 and v7


Stage IV Ovarian Embryonal Carcinoma AJCC v6 and v7


Metastatic Ovarian Clear Cell Adenocarcinoma


Stage IIB Ovarian Germ Cell Tumor AJCC v6 and v7


Recurrent Ovarian Transitional Cell Carcinoma


Recurrent Ovarian Undifferentiated Carcinoma


Stage I Ovarian Germ Cell Tumor AJCC v6 and v7


malignant sex cord stromal tumor of ovary


Refractory Ovarian Clear Cell Adenocarcinoma


Stage IB Ovarian Germ Cell Tumor AJCC v6 and v7


malignant non-dysgerminomatous germ cell tumor of ovary


Stage II Ovarian Polyembryoma AJCC v6 and v7


Stage IIIA Ovarian Germ Cell Tumor AJCC v6 and v7


Ovarian germ cell choriocarcinoma stage II


Recurrent BRCA- Associated Ovarian Carcinoma


Refractory Extrarenal Rhabdoid Tumor of the Ovary


Stage IIIB Ovarian Cancer AJCC v6 and v7


Refractory Ovarian Squamous Cell Carcinoma


Stage IV Ovarian Polyembryoma AJCC v6 and v7


Ovarian germ cell choriocarcinoma stage I


Poorly Differentiated Ovarian Sertoli-Leydig Cell Tumor


Stage I Ovarian Dysgerminoma AJCC v6 and v7


Ovarian Low Grade Endometrioid Stromal Sarcoma


Recurrent Malignant Ovarian Granulosa Cell Tumor


Refractory Ovarian Transitional Cell Carcinoma


Stage IIA Ovarian Germ Cell Tumor AJCC v6 and v7


Metastatic Ovarian Endometrioid Adenocarcinoma


Metastatic Ovarian Small Cell Carcinoma, Hypercalcemic Type


Stage III Ovarian Polyembryoma AJCC v6 and v7


Stage III Ovarian Dysgerminoma AJCC v6 and v7


Refractory Malignant Ovarian Brenner Tumor


Stage II Ovarian Yolk Sac Tumor AJCC v6 and v7


Childhood Malignant Ovarian Germ Cell Tumor


Unresectable Ovarian Endometrioid Adenocarcinoma


Refractory Ovarian Mucinous Adenocarcinoma


Recurrent Ovarian Seromucinous Carcinoma


Recurrent Platinum-Resistant Ovarian Carcinoma


Stage II Ovarian Dysgerminoma AJCC v6 and v7


Refractory Ovarian Undifferentiated Carcinoma


Metastatic Ovarian Undifferentiated Carcinoma


Recurrent Ovarian Endometrioid Adenocarcinoma


Stage IV Ovarian Germ Cell Tumor AJCC v6 and v7


Metastatic Microsatellite Stable Ovarian Carcinoma


Stage IV Ovarian Dysgerminoma AJCC v6 and v7


Stage IA Ovarian Germ Cell Tumor AJCC v6 and v7


Metastatic Platinum-Resistant Ovarian Carcinoma


Recurrent Ovarian Clear Cell Adenocarcinoma


Metastatic Ovarian Mucinous Adenocarcinoma


Stage I Ovarian Polyembryoma AJCC v6 and v7


Refractory Ovarian Endometrioid Adenocarcinoma


Stage IV Ovarian Yolk Sac Tumor AJCC v6 and v7


Poorly Differentiated Ovarian Sertoli-Leydig Cell Tumor, Variant with Heterologous Elements


Stage I Ovarian Yolk Sac Tumor AJCC v6 and v7


Stage IIC Ovarian Germ Cell Tumor AJCC v6 and v7


Stage I Ovarian Embryonal Carcinoma AJCC v6 and v7


Recurrent Extrarenal Rhabdoid Tumor of the Ovary


Stage III Ovarian Embryonal Carcinoma AJCC v6 and v7


Stage II Ovarian Germ Cell Tumor AJCC v6 and v7


Recurrent Ovarian Mucinous Adenocarcinoma


Solid Pseudopapillary Neoplasm of the Ovary


Ovarian germ cell choriocarcinoma stage III


Unresectable Ovarian Undifferentiated Carcinoma


Stage III Ovarian Yolk Sac Tumor AJCC v6 and v7


Refractory Ovarian Seromucinous Carcinoma


Stage IIIC Ovarian Germ Cell Tumor AJCC v6 and v7


Unresectable Ovarian Mucinous Adenocarcinoma


Stage III Ovarian Germ Cell Tumor AJCC v6 and v7


Stage II Ovarian Embryonal Carcinoma AJCC v6 and v7


Unresectable Platinum-Resistant Ovarian Carcinoma


Ovarian germ cell choriocarcinoma stage IV


Stage IB Uterine Corpus Endometrial Stromal Sarcoma AJCC v8


congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency


autosomal recessive non-syndromic intellectual disability


PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome


metachromatic leukodystrophy, adult form


homocystinuria without methylmalonic aciduria


uterine corpus endometrial stromal sarcoma


autoimmune disorder of musculoskeletal system


combined oxidative phosphorylation deficiency


Pelizaeus-Merzbacher disease, transitional form


non-syndromic male infertility due to sperm motility disorder


developmental anomaly of metabolic origin


non-acquired pituitary hormone deficiency


glycerol kinase deficiency, infantile form


isolated oxidative phosphorylation complex disorder


atypical hemolytic-uremic syndrome with anti-factor H antibodies


autoimmune disorder of the nervous system


hypogonadotropic hypogonadism 17 with or without anosmia


Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2


diaphragmatic or abdominal wall malformation


classic congenital lipoid adrenal hyperplasia due to STAR deficency


Rubinstein-Taybi syndrome due to 16p13.3 microdeletion


disorder of phospholipids, sphingolipids and fatty acids biosynthesis


cerebral sclerosis similar to Pelizaeus-Merzbacher disease


disorder of development or morphogenesis


peroxisome biogenesis disorder due to PEX1 defect


qualitative or quantitative protein defects in neuromuscular diseases


inborn disorder of serine family metabolism


inborn disorder of phenylalanine and tyrosine metabolism


autoimmune disorder of peripheral nervous system


classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, simple virilizing form


Prader-Willi syndrome due to paternal 15q11q13 deletion


Grn-related frontotemporal lobar degeneration with Tdp43 inclusions


inborn disorder of gamma-aminobutyric acid metabolism


tumor of hematopoietic and lymphoid tissues


alanine glyoxylate aminotransferase deficiency


inborn disorder of pyrimidine metabolism


inherited renal cancer-predisposing syndrome


neurodegeneration with brain iron accumulation


colobomatous microphthalmia - obesity - hypogenitalism - intellectual disability syndrome


microcephalic osteodysplastic primordial dwarfism type II


nephropathy secondary to a storage or other metabolic disease


disorder of metabolite absorption and transport


inborn disorder of amino acid and other organic acid metabolism


inborn disorder of amino acid metabolism


hyperlysinemia due to defect in lysine transport into mitochondria


hypogonadotropic hypogonadism 14 with or without anosmia


MELAS syndrome caused by mutation in MTTQ


acquired chronic primary adrenal insufficiency


visceral malformation of the liver, biliary tract, pancreas or spleen


Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1


disorder of carbohydrate transmembrane transport and absorption


hypogonadotropic hypogonadism 22 with or without anosmia


MELAS syndrome caused by mutation in MTND1


malignant dysgerminomatous germ cell tumor of ovary


Pelizaeus-Merzbacher disease in female carriers


malignant germ cell tumor of cervix uteri


psoriasis-related juvenile idiopathic arthritis


necrotizing encephalomyelopathy, subacute, of Leigh, adult


disorder of folate metabolism and transport


inborn disorder of ornithine or proline metabolism


Wolman disease with hypolipoproteinemia and acanthocytosis


inborn disorder of pyridoxine metabolism


craniosynostosis syndrome, autosomal recessive


severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency


primary non-gestational choriocarcinoma of ovary


46,XX disorder of sex development induced by androgens excess


theca steroid-producing cell malignant tumor of ovary, not further specified


developmental and epileptic encephalopathy


mucopolysaccharidosis or mucopolysaccharidosis-like disorder


autosomal recessive degenerative and progressive cerebellar ataxia


autosomal recessive metabolic cerebellar ataxia


pseudoxanthomatous diffuse cutaneous mastocytosis


inborn disorder of neurotransmitter metabolism and transport


quantitative and/or qualitative congenital phagocyte defect


paternal 14q32.2 hypomethylation syndrome


familial adrenal hypoplasia with absent pituitary luteinizing hormone


pyruvate carboxylase deficiency, severe neonatal type


obesity due to melanocortin 4 receptor deficiency


inborn disorder of tryptophan metabolism


primordial dwarfism and slender bone disorder


mitochondrial oxidative phosphorylation disorder


sickle cell disease and related diseases


unspecified inborn mitochondrial disorder


pyruvate carboxylase deficiency, benign type


inborn disorder of lysine and hydroxylysine metabolism


anomaly of puberty or/and menstrual cycle of genetic origin


metabolic disease involving other neurotransmitter deficiency


familial primary hypomagnesemia with normocalcuria


cognitive impairment - coarse facies - heart defects - obesity - pulmonary involvement - short stature - skeletal dysplasia syndrome


disorder of iron metabolism and transport


systemic-onset juvenile idiopathic arthritis


MELAS syndrome caused by mutation in MTTC


multiple congenital anomalies/dysmorphic syndrome without intellectual disability


disorder of vitamin and non-protein cofactor absorption and transport


hematopoietic and lymphoid cell neoplasm


familial hyperreninemic hypoaldosteronism type 1


Huntington disease and related disorders


hypogonadotropic hypogonadism 21 with or without anosmia


pure or complex hereditary spastic paraplegia


disorder of other vitamins and cofactors metabolism and transport


high-grade neuroendocrine carcinoma of the cervix uteri


mild phosphoribosylpyrophosphate synthetase superactivity


hypogonadotropic hypogonadism 19 with or without anosmia


MELAS syndrome caused by mutation in MTND5


early-onset autosomal dominant Alzheimer disease


hyperphenylalaninemia due to DNAJC12 deficiency


infantile Bartter syndrome with sensorineural deafness


disorder of carnitine cycle and carnitine transport


46,XX disorder of sex development induced by fetal androgens excess


hypogonadotropic hypogonadism 20 with or without anosmia


autoimmune primary adrenal insufficiency


inherited glutathione metabolism disease


inborn disorder of biogenic amine metabolism and transport


inborn disorder of cobalamin metabolism and transport


atypical hemolytic-uremic syndrome with H factor anomaly


pure or complex autosomal dominant spastic paraplegia


tetrahydrobiopterin metabolic process disease


non-classic congenital lipoid adrenal hyperplasia due to STAR deficency


congenital disorder of glycosylation type I


ichthyosis, X-linked, without steroid sulfatase deficiency


maternal uniparental disomy of chromosome 14


mitochondrial DNA depletion syndrome, encephalomyopathic form


disorder of galactose and fructose metabolism


primitive neuroectodermal tumor of the cervix uteri


isolated congenital hypogonadotropic hypogonadism


hereditary disorder of connective tissue


peroxisomal single enzyme/protein defect


inborn disorder of methionine cycle and sulfur amino acid metabolism


adrenocortical hypofunction, chronic primary congenital


obesity due to pro-opiomelanocortin deficiency


qualitative or quantitative defects of dystrophin


46,XX disorder of sex development induced by fetoplacental androgens excess


neurometabolic disorder due to serine deficiency


multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome


inborn disorder of the gamma-glutamyl cycle


inborn disorder of pentose phosphate metabolism


combined pituitary hormone deficiencies, genetic form


endometrioid stromal sarcoma of the vagina


disorder of mineral absorption and transport


familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis


neonatal period electroclinical syndrome


inborn disorder of purine or pyrimidine metabolism


intellectual disability-obesity-brain malformations-facial dysmorphism syndrome


mitochondrial membrane transport disorder


disorder of beta and omega amino acid metabolism


neonatal-onset developmental and epileptic encephalopathy


non-classic congenital adrenal hyperplasia


MELAS syndrome caused by mutation in MTTS2


gamma-amino butyric acid metabolism disorder


urea cycle disorder or inherited hyperammonemia


MELAS syndrome caused by mutation in MTTK


hereditary site-specific ovarian cancer syndrome


primary immunodeficiency due to a defect in adaptive immunity


malignant Sertoli-Leydig cell tumor of ovary


intellectual disability-obesity-prognathism-eye and skin anomalies syndrome


MELAS syndrome caused by mutation in MTND6


frontotemporal dementia, right temporal atrophy variant


Pelizaeus-Merzbacher disease, connatal form


Prader-Willi syndrome due to translocation


MELAS syndrome caused by mutation in MTTH


polyarticular juvenile rheumatoid arthritis


46,XY disorder of sex development due to isolated 17,20-lyase deficiency


behavioral variant of frontotemporal dementia


Prader-Willi syndrome due to imprinting mutation


inclusion body myopathy with Paget disease of bone and frontotemporal dementia


Alzheimer disease, familial early-onset, with coexisting amyloid and prion pathology


metachromatic leukodystrophy, late infantile form


severe phosphoribosylpyrophosphate synthetase superactivity


MELAS syndrome caused by mutation in MTTL1


MELAS syndrome caused by mutation in MTTS1


inborn disorder of aspartate family metabolism


46,XY disorder of sex development of endocrine origin


inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency


peroxisome biogenesis disorder due to PEX7 defect


adrenocortical unresponsiveness to ACTH with postreceptor defect


inborn mitochondrial metabolism disorder


inborn disorder of lysosomal amino acid transport


primary bone dysplasia with increased bone density


multiple congenital anomalies/dysmorphic syndrome


congenital nonspherocytic hemolytic anemia


sulfite oxidase deficiency due to molybdenum cofactor deficiency


myopathy, lactic acidosis, and sideroblastic anemia


infectious disease or post-infectious disorder


encephalopathy due to sulfite oxidase deficiency


infectious disorder of the nervous system


inborn disorder of branched-chain amino acid metabolism


vitamin B12- and folate-independent constitutional megaloblastic anemia


endometrioid stromal sarcoma of the cervix


pyruvate carboxylase deficiency, infantile form


short stature-brachydactyly-obesity-global developmental delay syndrome


classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, salt wasting form


primary immunodeficiency due to a genetic defect in innate immunity


Alzheimer disease without neurofibrillary tangles


disorder of peptide and amine metabolism


mitochondrial substrate carrier disorder


recurrent infections-inflammatory syndrome due to zinc metabolism disorder syndrome


multiple congenital anomalies/dysmorphic syndrome-intellectual disability


Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15


hypogonadotropic hypogonadism 18 with or without anosmia


osteogenesis imperfecta and a reduction of bone mineral density.


disorder of fatty acid and ketone body metabolism


anomaly of puberty or/and menstrual cycle


obesity due to leptin receptor gene deficiency


glycerol kinase deficiency, juvenile form


X-linked syndromic intellectual disability


disorder of thiamine metabolism and transport


malignant mixed epithelial and mesenchymal tumor of cervix uteri


Pelizaeus-Merzbacher disease, classic form


peroxisome biogenesis disorder due to PEX12 defect


Stage IIIB Uterine Corpus Endometrial Stromal Sarcoma AJCC v8


Mismatch Repair-Deficient Endometrial Endometrioid Adenocarcinoma


4-(2-phenylethylsulfamoyl)-1H-pyrrole-2-carboxylic acid methyl ester


Stage IA Hepatocellular Carcinoma AJCC v8


Stage I Hepatocellular Carcinoma AJCC v8


Stage IB Hepatocellular Carcinoma AJCC v8


Extramedullary Disease in Plasma Cell Myeloma Involving the Liver


Localized Resectable Adult Hepatocellular Carcinoma


Refractory Endometrial Dedifferentiated Carcinoma


Cervical Mucinous Adenocarcinoma, Not Otherwise Specified


BCLC Stage 0 Adult Hepatocellular Carcinoma


1alpha,25-dihydroxy-22-oxavitamin D3 3-hemiglutarate/1alpha,25-dihydroxy-22-oxacholecalciferol 3-hemiglutarate


(6R)-vitamin D2 6,19-sulfur dioxide adduct/(6R)-ergocalciferol 6,19-sulfur dioxide adduct


(6R)-vitamin D3 6,19-(4-phenyl-1,2,4-triazoline-3,5-dione) adduct/(6R)-cholecalciferol 6,19-(4-phenyl-1,2,4-triazoline-3,5-dione) adduct


(5Z)-1alpha,25-dihydroxy-3-deoxy-3-thiavitamin D3 3-oxide/(5Z)-1alpha,25-dihydroxy-3-deoxy-3-thiacholecalciferol 3-oxide


1alpha-hydroxy-25,26,27-trinorvitamin D3 24-carboxylic acid


(23S,25R)-25-hydroxyvitamin D3 26,23-lactol/(23S,25R)-25-hydroxycholecalciferol 26,23-lactol


1alpha,25-Dihydroxyvitamin D3 25-trimethylsilyl ether


Extramedullary Disease in Plasma Cell Myeloma Involving the Spleen


Adenoma of the Colon with Intramucosal Adenocarcinoma


Colorectal Adenocarcinoma Metastatic in the Liver


Stage I Colorectal Cancer AJCC v6 and v7


Metastatic Malignant Colorectal Neoplasm


Rectal Carcinoma Metastatic in the Liver


Microsatellite Stable Colorectal Carcinoma


Colorectal Cribriform Comedo-Type Adenocarcinoma


Stage 0 Rectosigmoid Cancer AJCC v6 and v7


Colorectal Mixed Adenoneuroendocrine Carcinoma


Colorectal Small Cell Neuroendocrine Carcinoma


Metastatic Microsatellite Stable Colon Carcinoma


Inflammatory Bowel Disease-Associated Colorectal Adenocarcinoma


Ulcerative Colitis-Associated Colorectal Adenocarcinoma


malignant neoplasm of large intestine stage IV


Metastatic Colorectal Mucinous Adenocarcinoma


Colorectal Large Cell Neuroendocrine Carcinoma


Colon Large Cell Neuroendocrine Carcinoma


Colorectal Carcinoma Metastatic in the Liver


Colon Cribriform Comedo-Type Adenocarcinoma


Refractory Microsatellite Stable Colorectal Carcinoma


Crohn Disease-Associated Colorectal Adenocarcinoma


Locally Advanced Microsatellite Stable Colorectal Carcinoma


Metastatic malignant neoplasm to large intestine


Rectal Small Cell Neuroendocrine Carcinoma


Stage 0 Colorectal Cancer AJCC v6 and v7


Locally Advanced Microsatellite Stable Colon Carcinoma


Stage I Rectosigmoid Cancer AJCC v6 and v7


Rectal Cribriform Comedo-Type Adenocarcinoma


Refractory Rectal Squamous Cell Carcinoma


Metastatic Microsatellite Stable Colorectal Carcinoma


Rectal Large Cell Neuroendocrine Carcinoma


Colorectal Poorly Cohesive Adenocarcinoma


Advanced Microsatellite Stable Colorectal Carcinoma


Chronic obstructive asthma (with obstructive pulmonary disease)


Extramedullary Disease in Plasma Cell Myeloma Involving the Central Nervous System


Plasma Cell Myeloma Post-Transplant Lymphoproliferative Disorder


Extramedullary Disease in Plasma Cell Myeloma


Extramedullary Disease in Plasma Cell Myeloma Involving the Uterine Corpus


Extramedullary Disease in Plasma Cell Myeloma Involving the Skin


Extramedullary Disease in Plasma Cell Myeloma Involving the Kidney


Finding by Site or System

biolink:PhenotypicFeature biolink:DiseaseOrPhenotypicFeature biolink:ThingWithTaxon biolink:BiologicalEntity biolink:NamedThing biolink:Entity


Congenital isolated adrenocorticotropic hormone deficiency


Acquired Adrenocorticotropic Hormone Deficiency


Metastatic Endometrial Adenosquamous Carcinoma


Metastatic Cervical Adenosquamous Carcinoma


Recurrent Cervical Adenosquamous Carcinoma


Recurrent Endometrial Adenosquamous Carcinoma


Recurrent Endometrial Undifferentiated Carcinoma


Refractory Endometrial Undifferentiated Carcinoma


Stage IVA Uterine Corpus Endometrial Stromal Sarcoma AJCC v8


Uterine Corpus High Grade Endometrial Stromal Sarcoma


Cervical Malignant Peripheral Nerve Sheath Tumor


Stage I Uterine Corpus Endometrial Stromal Sarcoma AJCC v8


Stage IIIC Uterine Corpus Endometrial Stromal Sarcoma AJCC v8


Uterine Corpus Low Grade Endometrial Stromal Sarcoma


Stage IIIA Uterine Corpus Endometrial Stromal Sarcoma AJCC v8


Stage IVB Uterine Corpus Endometrial Stromal Sarcoma AJCC v8


Uterine Corpus Endometrial Stromal Sarcoma by AJCC v8 Stage


Stage II Uterine Corpus Endometrial Stromal Sarcoma AJCC v8


Stage IV Uterine Corpus Endometrial Stromal Sarcoma AJCC v8


Stage IA Uterine Corpus Endometrial Stromal Sarcoma AJCC v8


Stage III Uterine Corpus Endometrial Stromal Sarcoma AJCC v8


Cervical Low Grade Endometrioid Stromal Sarcoma


Stage III Hepatocellular Carcinoma AJCC v7


Hepatocellular Carcinoma by AJCC v7 Stage


Stage IIIC Hepatocellular Carcinoma AJCC v7


Stage IV Hepatocellular Carcinoma AJCC v7


Stage II Childhood Hepatocellular Carcinoma AJCC v6 and v7


Stage IVB Hepatocellular Carcinoma AJCC v7


Stage IVA Hepatocellular Carcinoma AJCC v7


Stage III Childhood Hepatocellular Carcinoma AJCC v7


Stage I Hepatocellular Carcinoma AJCC v6 and v7


Stage IIIA Hepatocellular Carcinoma AJCC v7


Stage II Hepatocellular Carcinoma AJCC v6 and v7


Stage IV Childhood Hepatocellular Carcinoma AJCC v7


Stage IIIB Hepatocellular Carcinoma AJCC v7


Stage I Childhood Hepatocellular Carcinoma AJCC v6 and v7


Refractory Endometrial Mucinous Adenocarcinoma


Refractory Microsatellite Stable Endometrial Carcinoma


Refractory Endometrial Endometrioid Adenocarcinoma


Metastatic Endometrial Mixed Cell Adenocarcinoma


Hepatocellular Carcinoma by AJCC v6 Stage


Well Differentiated Hepatocellular Carcinoma


Cervical Invasive Stratified Mucinous Adenocarcinoma


Stage IV Hepatocellular Carcinoma AJCC v6


High Grade Endometrial Endometrioid Adenocarcinoma


Human Papillomavirus-Related Cervical Squamous Cell Carcinoma


Metastatic Endometrial Clear Cell Adenocarcinoma


Human Papillomavirus-Related Cervical Adenocarcinoma In Situ


Stage III Cervical Cancer AJCC v6 and v7


Stage IVA Hepatocellular Carcinoma AJCC v8


Endometrial Mucinous Adenocarcinoma, Intestinal-Type


Hepatitis Virus-Related Hepatocellular Carcinoma


Non-Neoplastic Central Nervous System Disorder


Metastatic Malignant Neoplasm to the Cervix


Recurrent Endometrial Squamous Cell Carcinoma


Adult Pleomorphic Hepatocellular Carcinoma


POLE-Ultramutated Endometrial Endometrioid Adenocarcinoma


Moderately Differentiated Hepatocellular Carcinoma


Non-Neoplastic Genitourinary System Disorder


Human Papillomavirus-Independent Cervical Squamous Cell Carcinoma


p53-Mutant Endometrial Endometrioid Adenocarcinoma


Metastatic Microsatellite Stable Endometrial Carcinoma


Microsatellite Stable Endometrial Carcinoma


Non-Neoplastic Peritoneal and Retroperitoneal Disorder


Poorly Differentiated Hepatocellular Carcinoma


Recurrent Endometrial Mixed Cell Adenocarcinoma


Locally Advanced Cervical Squamous Cell Carcinoma


Recurrent Endometrial Mucinous Adenocarcinoma


Endometrial Large Cell Neuroendocrine Carcinoma


Cervical Squamous Cell Carcinoma In Situ


Human Papillomavirus-Independent Cervical Adenocarcinoma


Respiratory, thoracic and mediastinal disorders


Refractory Cervical Squamous Cell Carcinoma, Not Otherwise Specified


Stage IIIA Hepatocellular Carcinoma AJCC v8


Cervical Adenocarcinoma, Not Otherwise Specified


Metastatic Endometrial Serous Adenocarcinoma


Recurrent Adult Hepatocellular Carcinoma


BCLC Stage A Adult Hepatocellular Carcinoma


Human Papillomavirus-Related Cervical Adenocarcinoma


Macrotrabecular Massive Hepatocellular Carcinoma


Abnormal Blood Chemistry and Hematology Test Result


Peritoneal and retroperitoneal disorders


Hepatocellular carcinoma, spindle cell variant


Non-Neoplastic Digestive System Disorder


Recurrent Malignant Endocervical Neoplasm


Recurrent Cervical Squamous Cell Carcinoma


FIGO Grade 2 Endometrial Mucinous Adenocarcinoma


Endometrial Mucinous Adenocarcinoma, Gastric-Type


Hepatitis B Virus-Related Hepatocellular Carcinoma


Recurrent Endometrial Endometrioid Adenocarcinoma


Stage IIB Cervical Cancer AJCC v6 and v7


Refractory Endometrial Serous Adenocarcinoma


Recurrent Endometrial Dedifferentiated Carcinoma


Metastatic Cervical Squamous Cell Carcinoma


Utricle-Associated Mucosal Gland Hyperplasia


Unresectable Cervical Squamous Cell Carcinoma


Prostatic Clear Cell Cribriform Hyperplasia


Recurrent Endometrial Clear Cell Adenocarcinoma


AIDS-Related Malignant Cervical Neoplasm


No Specific Molecular Profile Endometrial Endometrioid Adenocarcinoma


Stage IV Hepatocellular Carcinoma AJCC v8


Refractory Endometrial Transitional Cell Carcinoma


Refractory Endometrial Squamous Cell Carcinoma


21-hydroxylase deficiency - simple virilizing


Non-Neoplastic Endocrine Pancreas Disorder


Non-Neoplastic Disorder by Special Category


Endometrial Endometrioid Adenocarcinoma with Clear Cell Change


Stage IVB Hepatocellular Carcinoma AJCC v8


Refractory Cervical Squamous Cell Carcinoma


Human Papillomavirus-Independent Cervical Adenocarcinoma In Situ


Endometrioid adenocarcinoma, ciliated cell variant


Stage III Hepatocellular Carcinoma AJCC v8


Refractory Endometrial Clear Cell Adenocarcinoma


FIGO Grade 2 Endometrial Endometrioid Adenocarcinoma


Mental and Behavioral Signs and Symptoms


Stage IVA Cervical Cancer AJCC v6 and v7


Cervical Adenocarcinoma Admixed with Neuroendocrine Carcinoma


Metastatic Endometrial Endometrioid Adenocarcinoma


Serous Endometrial Intraepithelial Carcinoma


Recurrent Endocervical Adenocarcinoma, Usual-Type


Stage II Hepatocellular Carcinoma AJCC v8


Human Papillomavirus-Related Cervical Carcinoma


Endometrial Endometrioid Adenocarcinoma with a Poorly Differentiated Carcinomatous Component


Stage IIIB Cervical Cancer AJCC v6 and v7


Female Non-Neoplastic Reproductive System Disorder


Non-Neoplastic Connective and Soft Tissue Disorder


BCLC Stage C Adult Hepatocellular Carcinoma


Stage III Hepatocellular Carcinoma AJCC v6


Stage IVB Cervical Cancer AJCC v6 and v7


Metastatic Carcinoma to the Uterine Cervix


Low Grade Endometrial Endometrioid Adenocarcinoma


FIGO Grade 1 Endometrial Mucinous Adenocarcinoma


Stage IIIB Hepatocellular Carcinoma AJCC v8


Cutaneous Hematopoietic and Lymphoid Cell Neoplasm


Cervix Intraepithelial Neoplasia Grade 3 AJCC v7


Locally Advanced Cervical Adenocarcinoma


Schizophrenia and other psychotic disorders


Hepatocellular Carcinoma by AJCC v8 Stage


Recurrent Endometrial Transitional Cell Carcinoma


Endometrial Endometrioid Adenocarcinoma with an Undifferentiated Carcinomatous Component


Recurrent Childhood Hepatocellular Carcinoma


FIGO Grade 1 Endometrial Endometrioid Adenocarcinoma


Small Progressed Hepatocellular Carcinoma


Non-Neoplastic Hematologic and Lymphocytic Disorder


Cervical Papillary Squamous Cell Carcinoma


Recurrent Endometrial Serous Adenocarcinoma


Locally Advanced Hepatocellular Carcinoma


BCLC Stage B Adult Hepatocellular Carcinoma


Localized Unresectable Adult Hepatocellular Carcinoma


BCLC Stage D Adult Hepatocellular Carcinoma


Refractory Endometrial Mixed Cell Adenocarcinoma


Hepatitis C Virus-Related Hepatocellular Carcinoma


Cervical Squamous Cell Carcinoma, Not Otherwise Specified


FIGO Grade 3 Endometrial Mucinous Adenocarcinoma


Non-Neoplastic Respiratory System Disorder


uridine 5'-[3-(L-rhamnopyranosyl) dihydrogen diphosphate]


4-[dimethylamino(oxo)methyl]-3,5-dimethyl-1H-pyrrole-2-carboxylic acid ethyl ester


diammonium (2R)-3-[(12-aminododecanoyl)oxy]-2-(palmitoyloxy)propyl (2R)-2,3-bis(palmitoyloxy)propyl 2-hydroxypropane-1,3-diyl bis(phosphate)


Aurintricarboxylic acid triammonium salt


5-[Diethylamino(oxo)methyl]-4-methyl-2-(1-oxopentylamino)-3-thiophenecarboxylic acid methyl ester


5-[[3-(1,5-dimethyl-4-pyrazolyl)-1-oxoprop-2-enyl]amino]-3-methylthiophene-2,4-dicarboxylic acid O2-ethyl ester O4-propan-2-yl ester


1-(4-Amino-1,2,5-oxadiazol-3-yl)-5-[(2-pyridinylthio)methyl]-4-triazolecarboxylic acid propan-2-yl ester


3-[[2-(2-Chloro-4-fluorophenoxy)-1-oxoethyl]amino]-2-thiophenecarboxylic acid methyl ester


L-Citrulline-5,5-d2, 97 atom % D (partial deuteration at C4), 97% (CP)


2-(3-Formyl-2,5-dimethyl-1-pyrrolyl)-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylic acid methyl ester


2-[(4,4-Dimethyl-2,6-dioxocyclohexyl)methylideneamino]-5-methyl-3-thiophenecarboxylic acid ethyl ester


2-Propenoic acid, 3-(4-hydroxyphenyl)-, (2Z)-


2-Thiophenecarboxylic acid [2-oxo-2-(2-oxolanylmethylamino)ethyl] ester


3-(Tert-butylsulfamoyl)-4-phenyl-5-(trifluoromethyl)-2-thiophenecarboxylic acid methyl ester


dicarboxylic acids and O-substituted derivatives


2-Thiophenecarboxylic acid [1-[2-(4-methoxyphenyl)cyclopropyl]ethylideneamino] ester


erythrose 4-phosphate/phosphoenolpyruvate family amino acid


4-(5-methyl-2-furanyl)-2-[[1-oxo-2-(1H-1,2,4-triazol-5-ylthio)ethyl]amino]-3-thiophenecarboxylic acid ethyl ester


Propanedioic acid, (methoxyimino)-, dimethyl ester


3-[5-[Oxo-(3-pyridinylamino)methyl]-2-furanyl]-2-thiophenecarboxylic acid methyl ester


2-[(1-Oxo-3-phenylpropyl)amino]-3-thiophenecarboxylic acid methyl ester


2-[[2-[(ethoxycarbonylamino)-oxomethyl]-3-oxobut-1-enyl]amino]-3-thiophenecarboxylic acid methyl ester


5-[2-(5-Methoxycarbonyl-2-thiophenyl)butan-2-yl]-2-thiophenecarboxylic acid methyl ester


2-[[[(6-Methyl-2-pyridinyl)amino]-sulfanylidenemethyl]amino]-5-phenyl-3-thiophenecarboxylic acid ethyl ester


3-Methyl-2-thiophenecarboxylic acid [2-(4-morpholinyl)-2-oxoethyl] ester


Benzoic acid, 4-amino-, 4-acetoxy-2,2,6,6-tetramethyl-1-piperidinyl ester


8-Methylsulfinyl-4,5-dihydrothieno[3,4-g][2,1]benzoxazole-6-carboxylic acid ethyl ester


4,5-Dimethyl-2-[[1-oxo-2-[4-(phenylmethyl)-1-pyridin-1-iumyl]ethyl]amino]-3-thiophenecarboxylic acid ethyl ester


L-Aspartic acid-d7, 98 atom % D, 98% (CP)


2-Thiophenecarboxylic acid [[amino-(2-methylphenyl)methylidene]amino] ester


2-(Methanesulfonamido)-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylic acid methyl ester


4-Cyclopropyl-2-[[2-[(3,5-dimethyl-4-isoxazolyl)methylthio]-1-oxoethyl]amino]-3-thiophenecarboxylic acid ethyl ester


2-[[(4-Bromo-1-ethyl-3-pyrazolyl)-oxomethyl]amino]-4-phenyl-3-thiophenecarboxylic acid ethyl ester


2-Thiophenecarboxylic acid [3-methyl-1-oxo-1-(thiophen-2-ylmethylamino)butan-2-yl] ester


2-[[2-furanyl(oxo)methyl]amino]-5,6-dihydro-4H-cyclopenta[b]thiophene-3-carboxylic acid methyl ester


2-[[Acetamido(sulfanylidene)methyl]amino]-5-ethyl-3-thiophenecarboxylic acid ethyl ester


4-[(3-Cyano-4,6-dimethyl-2-pyridinyl)thio]-3-oxobutanoic acid propan-2-yl ester


3-[[Cyclopropyl(oxo)methyl]amino]-5-phenyl-2-thiophenecarboxylic acid methyl ester


1-Methyl-4-piperidyl benzhydryl ether hydrochloride


Benzenaminium, 4-[[4-(dimethylamino)phenyl][4-(dimethyliminio)-2,5-cyclohexadien-1-ylidene]methyl]-N-ethyl-N,N-dimethyl-, bromide chloride (1:1:1)


L-Phenylalanine, N-(3,5-dichloro-2-hydroxy-4-(2-(4-methyl-1-piperazinyl)ethoxy)benzoyl)-, ethyl ester, dihydrochloride


Copolymer of diethylenetriamine and 1-chloro-2,3-epoxypropane, hydrochloride


Guanosine 5'-(trihydrogen diphosphate) P'-D-mannopyranosyl ester


2-[[3-Cyano-6-cyclopropyl-4-(trifluoromethyl)-2-pyridinyl]thio]acetic acid methyl ester


2-[[7-(4-Methoxyphenyl)-5-phenyl-4-pyrrolo[2,3-d]pyrimidinyl]thio]propanoic acid ethyl ester


N-(very-long-chain fatty acyl)-sphingoid base


6-(3,4-Dimethoxyphenyl)-4-oxo-3-phenyl-1,5,6,7-tetrahydroindole-2-carboxylic acid ethyl ester


1-[3-[2-(Dimethylamino)ethylamino]-3-oxopropyl]-2-methyl-5-(4-methylphenyl)-3-pyrrolecarboxylic acid ethyl ester


4-Hydroxybenzoic acid [2-[1-(2-fluorophenyl)-2,5-dimethyl-3-pyrrolyl]-2-oxoethyl] ester


2-Methyl-4-phenyl-1H-pyrrole-3-carboxylic acid methyl ester


N-[[1-(4-fluorophenyl)-2,5-dimethyl-3-pyrrolyl]methylideneamino]carbamic acid methyl ester


3-(3-Formyl-2,5-dimethyl-1-pyrrolyl)-4-methylbenzoic acid methyl ester


Pyrrolidinium, 3-(((2S)-cyclopentylhydroxyphenylacetyl)oxy)-1,1-dimethyl-, bromide, (3R)-


N-[3-carbamoyl-5-[diethylamino(oxo)methyl]-4-methyl-2-thiophenyl]carbamic acid methyl ester


5-Amino-3-(4-methoxyphenyl)-7-methyl-4-oxo-1-thieno[3,4-d]pyridazinecarboxylic acid methyl ester


5-Nitro-2-thiophenecarboxylic acid [2-oxo-2-[(phenylmethyl)amino]ethyl] ester


5-[(Cyclohexylamino)-oxomethyl]-4-methyl-2-[(1-oxo-2-thiophen-2-ylethyl)amino]-3-thiophenecarboxylic acid ethyl ester


5-Nitro-2-thiophenecarboxylic acid [2-oxo-2-[[oxo-[(phenylmethyl)amino]methyl]amino]ethyl] ester


4,5-Dimethyl-2-[[oxo(thiophen-2-yl)methyl]amino]-3-thiophenecarboxylic acid ethyl ester


N-[1-methyl-3-(trifluoromethyl)-5-thieno[2,3-c]pyrazolyl]carbamic acid 2,2-dimethylpropyl ester


5-Nitro-2-thiophenecarboxylic acid [2-oxo-2-(1-phenylethylamino)ethyl] ester


5-Nitro-2-thiophenecarboxylic acid [1-[(3,5-dichloro-2-pyridinyl)amino]-1-oxopropan-2-yl] ester


2-[[1-oxo-2-(1H-1,2,4-triazol-5-ylthio)ethyl]amino]-4-thiophen-2-yl-3-thiophenecarboxylic acid ethyl ester


Ethanethioic acid, S-(2,5-dimethyl-3-furanyl) ester


2-[(6-Amino-3,5-dicyano-4-thiophen-2-yl-2-pyridinyl)thio]acetic acid ethyl ester


2-[(6-Amino-3,5-dicyano-2-pyridinyl)thio]acetic acid ethyl ester


2-[[3-Cyano-6-(2-furanyl)-4-(trifluoromethyl)-2-pyridinyl]thio]propanoic acid ethyl ester


2-[(4-Methyl-5-sulfanylidene-1,3,4-thiadiazol-2-yl)thio]acetic acid ethyl ester


Benzoic acid [2-oxo-2-[2-(phenylthio)anilino]ethyl] ester


1-(4-Methoxyphenyl)-4-[(4-methylphenyl)thio]-6-oxo-3-pyridazinecarboxylic acid methyl ester


2-[[4-Methyl-5-(2-phenylethyl)-1,2,4-triazol-3-yl]thio]acetic acid methyl ester


2-[(2-sulfanylidene-3H-1,3,4-thiadiazol-5-yl)thio]propanoic acid methyl ester


2-[(5-Acetyl-3-cyano-6-methyl-2-pyridinyl)thio]acetic acid ethyl ester


4-[(3-cyano-6,7-dihydro-5H-cyclopenta[b]pyridin-2-yl)thio]-3-oxobutanoic acid ethyl ester


5-[2-[(4-chlorophenyl)thio]-1-oxoethyl]-2,4-dimethyl-1H-pyrrole-3-carboxylic acid methyl ester


3-[(2-sulfanylidene-3H-1,3,4-thiadiazol-5-yl)thio]propanoic acid ethyl ester


3-Amino-4-[(4-chlorophenyl)thio]benzoic acid methyl ester


2-[[4-Cyano-3-[(2-methoxy-2-oxoethyl)thio]-5-isothiazolyl]thio]acetic acid ethenyl ester


2-[[5-[[2-(3-Chloroanilino)-4-thiazolyl]methyl]-4-(3-methoxypropyl)-1,2,4-triazol-3-yl]thio]acetic acid methyl ester


2-(Phenylthio)acetic acid [[amino-(4-methylphenyl)methylidene]amino] ester


5-[2-[(4-chlorophenyl)thio]-1-oxoethyl]-2,4-dimethyl-1H-pyrrole-3-carboxylic acid ethyl ester


carbohydrates and carbohydrate derivatives


migraine with or without aura, susceptibility to