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 53401 - 53425 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C1859995 Hyperandrogenism, Nonclassic Type, due to 21-Hydroxylase Deficiency CYP21A2 1589 cytochrome P450 family 21 subfamily A member 2 P08686
C0008312 Primary biliary cirrhosis CYP21A2 1589 cytochrome P450 family 21 subfamily A member 2 P08686
C0025517 Metabolic Diseases CYP21A2 1589 cytochrome P450 family 21 subfamily A member 2 P08686
C0001624 Adrenal Gland Neoplasms CYP21A2 1589 cytochrome P450 family 21 subfamily A member 2 P08686
C3150275 COMPLEMENT COMPONENT 2 DEFICIENCY CYP21A2 1589 cytochrome P450 family 21 subfamily A member 2 P08686
C0343804 Chronic Chagas' disease CYP21A2 1589 cytochrome P450 family 21 subfamily A member 2 P08686
C0011854 Diabetes Mellitus, Insulin-Dependent CYP21A2 1589 cytochrome P450 family 21 subfamily A member 2 P08686
C0001623 Adrenal gland hypofunction CYP21A2 1589 cytochrome P450 family 21 subfamily A member 2 P08686
C2752038 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 4 CYP21A2 1589 cytochrome P450 family 21 subfamily A member 2 P08686
C0151779 Cutaneous Melanoma CYP21A2 1589 cytochrome P450 family 21 subfamily A member 2 P08686
C0405580 Adrenal cortical hypofunction CYP21A2 1589 cytochrome P450 family 21 subfamily A member 2 P08686
C1857276 Trichohepatoenteric Syndrome CYP21A2 1589 cytochrome P450 family 21 subfamily A member 2 P08686
C0018051 Gonadal Dysgenesis CYP21A2 1589 cytochrome P450 family 21 subfamily A member 2 P08686
C0271737 Addison's disease due to autoimmunity CYP21A2 1589 cytochrome P450 family 21 subfamily A member 2 P08686
C0017665 Membranous glomerulonephritis CYP21A2 1589 cytochrome P450 family 21 subfamily A member 2 P08686
C1269683 Major Depressive Disorder CYP21A2 1589 cytochrome P450 family 21 subfamily A member 2 P08686
C0028754 Obesity CYP21A2 1589 cytochrome P450 family 21 subfamily A member 2 P08686
C0162538 Immunoglobulin A deficiency (disorder) CYP21A2 1589 cytochrome P450 family 21 subfamily A member 2 P08686
C0152013 Adenocarcinoma of lung (disorder) CYP21A2 1589 cytochrome P450 family 21 subfamily A member 2 P08686
C0001403 Addison Disease CYP21A2 1589 cytochrome P450 family 21 subfamily A member 2 P08686
C0149745 Oral Ulcer CYP21A2 1589 cytochrome P450 family 21 subfamily A member 2 P08686
C0848558 Hypospadias CYP21A2 1589 cytochrome P450 family 21 subfamily A member 2 P08686
C0271084 Exudative age-related macular degeneration CYP21A2 1589 cytochrome P450 family 21 subfamily A member 2 P08686
C0010068 Coronary heart disease CYP21A2 1589 cytochrome P450 family 21 subfamily A member 2 P08686
C1153706 Endometrial adenocarcinoma CYP21A2 1589 cytochrome P450 family 21 subfamily A member 2 P08686

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Last updated: August 19, 2024