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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 |
|---|---|---|---|---|---|
| C2931132 | Crigler Najjar syndrome, type 2 | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
| C0018790 | Cardiac Arrest | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
| C0400966 | Non-alcoholic Fatty Liver Disease | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
| C0014544 | Epilepsy | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
| C0008370 | Cholestasis | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
| C0270210 | Lucey-Driscoll syndrome (disorder) | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
| C0678222 | Breast Carcinoma | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
| C0010324 | Crigler Najjar syndrome, type 1 | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
| C0008350 | Cholelithiasis | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
| C0857007 | Hyperbilirubinemia, Neonatal | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
| C0002875 | Cooley's anemia | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
| C0017551 | Gilbert Disease (disorder) | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
| C0235974 | Pancreatic carcinoma | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
| C0027947 | Neutropenia | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
| C0947622 | Cholecystolithiasis | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
| C0023530 | Leukopenia | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
| C2931132 | Crigler Najjar syndrome, type 2 | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
| C0036341 | Schizophrenia | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
| C0036572 | Seizures | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
| C0011226 | Hepatitis D Infection | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
| C1337013 | Differentiated Thyroid Gland Carcinoma | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
| C1306459 | Primary malignant neoplasm | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
| C0152013 | Adenocarcinoma of lung (disorder) | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
| C0346647 | Malignant neoplasm of pancreas | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
