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 |
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DisGeNET | July 29, 2024 |
Disease ID | Disease Name | Gene Symbol | Gene ID | Gene Name ▼ | UniProt ID |
---|---|---|---|---|---|
C0019572 | Hirsutism | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
C0221043 | Liddle Syndrome | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
C0027059 | Myocarditis | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
C0282160 | Aplasia Cutis Congenita | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
C0220766 | Congenital hypoplasia of adrenal gland | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
C0025517 | Metabolic Diseases | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
C0431663 | Bilateral Cryptorchidism | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
C1510586 | Autism Spectrum Disorders | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
C0027051 | Myocardial Infarction | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
C1378703 | Renal carcinoma | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
C0018418 | Gynecomastia | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
C0266362 | Ambiguous Genitalia | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
C0149516 | Chronic sinusitis | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
C0302280 | Adrenogenital Syndrome | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
C1857276 | Trichohepatoenteric Syndrome | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
C0004775 | Bartter Disease | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
C0001925 | Albuminuria | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
C0034013 | Precocious Puberty | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
C0015934 | Fetal Growth Retardation | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
C0085580 | Essential Hypertension | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
C0678222 | Breast Carcinoma | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
C0038454 | Cerebrovascular accident | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
C0029456 | Osteoporosis | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
C0018799 | Heart Diseases | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
C0020621 | Hypokalemia | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
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Last updated: August 19, 2024