DisGeNET

DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.

Source Last Updated
DisGeNET July 29, 2024
Displaying entries 53776 - 53800 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0003467 Anxiety CYP17A1 1586 cytochrome P450 family 17 subfamily A member 1 P05093
C0024299 Lymphoma CYP17A1 1586 cytochrome P450 family 17 subfamily A member 1 P05093
C0405580 Adrenal cortical hypofunction CYP17A1 1586 cytochrome P450 family 17 subfamily A member 1 P05093
C0004763 Barrett Esophagus CYP17A1 1586 cytochrome P450 family 17 subfamily A member 1 P05093
C1853926 NONAKA MYOPATHY CYP17A1 1586 cytochrome P450 family 17 subfamily A member 1 P05093
C0235782 Gallbladder Carcinoma CYP17A1 1586 cytochrome P450 family 17 subfamily A member 1 P05093
C0016977 Gall Bladder Diseases CYP17A1 1586 cytochrome P450 family 17 subfamily A member 1 P05093
C1852222 Failure of Tooth Eruption, Primary CYP17A1 1586 cytochrome P450 family 17 subfamily A member 1 P05093
C1384583 Congenital absence of germinal epithelium of testes CYP17A1 1586 cytochrome P450 family 17 subfamily A member 1 P05093
C0009402 Colorectal Carcinoma CYP17A1 1586 cytochrome P450 family 17 subfamily A member 1 P05093
C0011860 Diabetes Mellitus, Non-Insulin-Dependent CYP17A1 1586 cytochrome P450 family 17 subfamily A member 1 P05093
C0017636 Glioblastoma CYP17A1 1586 cytochrome P450 family 17 subfamily A member 1 P05093
C3277849 17,20-Lyase Deficiency, Isolated CYP17A1 1586 cytochrome P450 family 17 subfamily A member 1 P05093
C0016724 Froehlich's Syndrome CYP17A1 1586 cytochrome P450 family 17 subfamily A member 1 P05093
C1832232 Peroxisome Biogenesis Disorder, Complementation Group C CYP17A1 1586 cytochrome P450 family 17 subfamily A member 1 P05093
C0238339 Hereditary pancreatitis CYP17A1 1586 cytochrome P450 family 17 subfamily A member 1 P05093
C0848558 Hypospadias CYP17A1 1586 cytochrome P450 family 17 subfamily A member 1 P05093
C1956346 Coronary Artery Disease CYP17A1 1586 cytochrome P450 family 17 subfamily A member 1 P05093
C3489396 Hypogonadism, Isolated Hypogonadotropic CYP17A1 1586 cytochrome P450 family 17 subfamily A member 1 P05093
C1857276 Trichohepatoenteric Syndrome CYP17A1 1586 cytochrome P450 family 17 subfamily A member 1 P05093
C0015934 Fetal Growth Retardation CYP17A1 1586 cytochrome P450 family 17 subfamily A member 1 P05093
C0279000 Liver and Intrahepatic Biliary Tract Carcinoma CYP17A1 1586 cytochrome P450 family 17 subfamily A member 1 P05093
C0010417 Cryptorchidism CYP17A1 1586 cytochrome P450 family 17 subfamily A member 1 P05093
C0023267 Fibroid Tumor CYP17A1 1586 cytochrome P450 family 17 subfamily A member 1 P05093
C0015695 Fatty Liver CYP17A1 1586 cytochrome P450 family 17 subfamily A member 1 P05093

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Last updated: August 19, 2024