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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 |
| Disease ID | Disease Name | Gene Symbol | Gene ID | Gene Name | UniProt ID ▲ |
|---|---|---|---|---|---|
| C0002874 | Aplastic Anemia | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0740391 | Middle Cerebral Artery Occlusion | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C1720830 | Painful Bladder Syndrome | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0015934 | Fetal Growth Retardation | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0019158 | Hepatitis | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0878544 | Cardiomyopathies | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0004936 | Mental disorders | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0041296 | Tuberculosis | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0740394 | Hyperuricemia | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0011854 | Diabetes Mellitus, Insulin-Dependent | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0017154 | Gastritis, Atrophic | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0002886 | Anemia, Macrocytic | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0024115 | Lung diseases | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0007102 | Malignant tumor of colon | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0751951 | Central Core Myopathy (disorder) | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0156312 | Atrophy of testis | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0033578 | Prostatic Neoplasms | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
| C0476089 | Endometrial Carcinoma | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
| C0021364 | Male infertility | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
| C0006826 | Malignant Neoplasms | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
| C0029456 | Osteoporosis | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
| C0376358 | Malignant neoplasm of prostate | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
| C0014175 | Endometriosis | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
| C0242379 | Malignant neoplasm of lung | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
| C0268285 | Adrenal hyperplasia, congenital, type 5 | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
