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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 |
|---|---|---|---|---|---|
| C0027651 | Neoplasms | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
| C0004623 | Bacterial Infections | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
| C0011581 | Depressive disorder | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
| C3888088 | SMITH-MCCORT DYSPLASIA 1 | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
| C0040028 | Thrombocythemia, Essential | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
| C0242422 | Parkinsonian Disorders | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
| C0344315 | Depressed mood | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
| C0017606 | Primary angle-closure glaucoma | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
| C0002726 | Amyloidosis | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
| C0017605 | Angle Closure Glaucoma | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
| C0345904 | Malignant neoplasm of liver | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
| C0699885 | Carcinoma of bladder | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
| C0005684 | Malignant neoplasm of urinary bladder | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
| C0024713 | Manic Disorder | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
| C1306459 | Primary malignant neoplasm | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
| C0238395 | Male Pseudohermaphroditism | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
| C1856127 | Bile acid synthesis defect, congenital, 2 | AKR1D1 | 6718 | aldo-keto reductase family 1 member D1 | P51857 |
| C0019158 | Hepatitis | AKR1D1 | 6718 | aldo-keto reductase family 1 member D1 | P51857 |
| C0011849 | Diabetes Mellitus | AKR1D1 | 6718 | aldo-keto reductase family 1 member D1 | P51857 |
| C0000768 | Congenital Abnormality | AKR1D1 | 6718 | aldo-keto reductase family 1 member D1 | P51857 |
| C0019159 | Hepatitis A | AKR1D1 | 6718 | aldo-keto reductase family 1 member D1 | P51857 |
| C0392514 | Hereditary hemochromatosis | AKR1D1 | 6718 | aldo-keto reductase family 1 member D1 | P51857 |
| C0029456 | Osteoporosis | AKR1D1 | 6718 | aldo-keto reductase family 1 member D1 | P51857 |
| C0023895 | Liver diseases | AKR1D1 | 6718 | aldo-keto reductase family 1 member D1 | P51857 |
| C0024523 | Malabsorption Syndrome | AKR1D1 | 6718 | aldo-keto reductase family 1 member D1 | P51857 |
