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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 ▼ |
|---|---|---|---|---|---|
| C0010068 | Coronary heart disease | AKR1A1 | 10327 | aldo-keto reductase family 1 member A1 | P14550 |
| C0007131 | Non-Small Cell Lung Carcinoma | AKR1A1 | 10327 | aldo-keto reductase family 1 member A1 | P14550 |
| C0024305 | Lymphoma, Non-Hodgkin | AKR1A1 | 10327 | aldo-keto reductase family 1 member A1 | P14550 |
| C0001418 | Adenocarcinoma | AKR1A1 | 10327 | aldo-keto reductase family 1 member A1 | P14550 |
| C0699791 | Stomach Carcinoma | AKR1A1 | 10327 | aldo-keto reductase family 1 member A1 | P14550 |
| C0004364 | Autoimmune Diseases | AKR1A1 | 10327 | aldo-keto reductase family 1 member A1 | P14550 |
| C1956346 | Coronary Artery Disease | AKR1A1 | 10327 | aldo-keto reductase family 1 member A1 | P14550 |
| C0018784 | Sensorineural Hearing Loss (disorder) | AKR1A1 | 10327 | aldo-keto reductase family 1 member A1 | P14550 |
| C0281361 | Adenocarcinoma of pancreas | AKR1A1 | 10327 | aldo-keto reductase family 1 member A1 | P14550 |
| C0004238 | Atrial Fibrillation | AKR1A1 | 10327 | aldo-keto reductase family 1 member A1 | P14550 |
| C0520459 | Necrotizing Enterocolitis | AKR1A1 | 10327 | aldo-keto reductase family 1 member A1 | P14550 |
| C0153398 | Hypopharyngeal Cancer | AKR1A1 | 10327 | aldo-keto reductase family 1 member A1 | P14550 |
| C0162429 | Malnutrition | AKR1A1 | 10327 | aldo-keto reductase family 1 member A1 | P14550 |
| C0700345 | Candidiasis, Vulvovaginal | AKR1A1 | 10327 | aldo-keto reductase family 1 member A1 | P14550 |
| C0005695 | Bladder Neoplasm | AKR1A1 | 10327 | aldo-keto reductase family 1 member A1 | P14550 |
| C0271093 | Stargardt's disease | AKR1A1 | 10327 | aldo-keto reductase family 1 member A1 | P14550 |
| C0024523 | Malabsorption Syndrome | SI | 6476 | sucrase-isomaltase | P14410 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | SI | 6476 | sucrase-isomaltase | P14410 |
| C0020456 | Hyperglycemia | SI | 6476 | sucrase-isomaltase | P14410 |
| C0011849 | Diabetes Mellitus | SI | 6476 | sucrase-isomaltase | P14410 |
| C0017921 | Glycogen storage disease type II | SI | 6476 | sucrase-isomaltase | P14410 |
| C0011991 | Diarrhea | SI | 6476 | sucrase-isomaltase | P14410 |
| C0342751 | Generalized glycogen storage disease of infants | SI | 6476 | sucrase-isomaltase | P14410 |
| C0020615 | Hypoglycemia | SI | 6476 | sucrase-isomaltase | P14410 |
| C0026848 | Myopathy | SI | 6476 | sucrase-isomaltase | P14410 |
