Hirsutism Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Abnormally increased hair growth referring to a male pattern of body hair (androgenic hair). (Human Phenotype Ontology, HP_0001007)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D006628
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Genes

27 genes/proteins associated with the disease Hirsutism from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
POMC proopiomelanocortin 2.88009
LHB luteinizing hormone beta polypeptide 1.76289
FSHB follicle stimulating hormone, beta polypeptide 1.54523
AR androgen receptor 1.42047
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor) 1.28456
C3 complement component 3 1.27751
TNF tumor necrosis factor 1.20751
PKP4 plakophilin 4 1.19179
CYP17A1 cytochrome P450, family 17, subfamily A, polypeptide 1 1.18882
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1 1.1461
GREB1 growth regulation by estrogen in breast cancer 1 1.10493
HSD17B3 hydroxysteroid (17-beta) dehydrogenase 3 1.09262
IGF1 insulin-like growth factor 1 (somatomedin C) 1.07875
IGFBP3 insulin-like growth factor binding protein 3 1.07376
APOA1 apolipoprotein A-I 1.05052
F5 coagulation factor V (proaccelerin, labile factor) 1.04684
CYP3A cytochrome P450, family 3, subfamily A 1.03456
ALDH1A1 aldehyde dehydrogenase 1 family, member A1 1.03197
PLG plasminogen 1.02821
SERPINC1 serpin peptidase inhibitor, clade C (antithrombin), member 1 1.02783
POR P450 (cytochrome) oxidoreductase 1.01966
CXCL10 chemokine (C-X-C motif) ligand 10 1.0189
PLEKHB2 pleckstrin homology domain containing, family B (evectins) member 2 1.01814
NR1I2 nuclear receptor subfamily 1, group I, member 2 1.01549
CDKN2C cyclin-dependent kinase inhibitor 2C (p18, inhibits CDK4) 1.01474
KCTD3 potassium channel tetramerization domain containing 3 1.01286
CCDC50 coiled-coil domain containing 50 1.01212