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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 ▼ |
|---|---|---|---|---|---|
| C0079731 | B-Cell Lymphomas | CS | 1431 | citrate synthase | O75390 |
| C0017636 | Glioblastoma | CS | 1431 | citrate synthase | O75390 |
| C4721610 | Carcinoma, Ovarian Epithelial | CS | 1431 | citrate synthase | O75390 |
| C0015695 | Fatty Liver | CS | 1431 | citrate synthase | O75390 |
| C0031511 | Pheochromocytoma | CS | 1431 | citrate synthase | O75390 |
| C2711227 | Steatohepatitis | CS | 1431 | citrate synthase | O75390 |
| C0011847 | Diabetes | CS | 1431 | citrate synthase | O75390 |
| C0020459 | Hyperinsulinism | CS | 1431 | citrate synthase | O75390 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | CS | 1431 | citrate synthase | O75390 |
| C0451819 | Simple obesity | CS | 1431 | citrate synthase | O75390 |
| C0004352 | Autistic Disorder | CS | 1431 | citrate synthase | O75390 |
| C1140680 | Malignant neoplasm of ovary | CS | 1431 | citrate synthase | O75390 |
| C0020550 | Hyperthyroidism | CS | 1431 | citrate synthase | O75390 |
| C1456418 | Absence of muscle | CS | 1431 | citrate synthase | O75390 |
| C0919267 | ovarian neoplasm | CS | 1431 | citrate synthase | O75390 |
| C0017075 | Ganglioneuroma | CS | 1431 | citrate synthase | O75390 |
| C0011570 | Mental Depression | CS | 1431 | citrate synthase | O75390 |
| C0014118 | Endocarditis | CS | 1431 | citrate synthase | O75390 |
| C0151744 | Myocardial Ischemia | CS | 1431 | citrate synthase | O75390 |
| C0235527 | Heart Failure, Right-Sided | CS | 1431 | citrate synthase | O75390 |
| C0033860 | Psoriasis | CS | 1431 | citrate synthase | O75390 |
| C0221356 | Brachycephaly | MPDU1 | 9526 | mannose-P-dolichol utilization defect 1 | O75352 |
| C1836669 | CONGENITAL DISORDER OF GLYCOSYLATION, TYPE If | MPDU1 | 9526 | mannose-P-dolichol utilization defect 1 | O75352 |
| C0282577 | Congenital Disorders of Glycosylation | MPDU1 | 9526 | mannose-P-dolichol utilization defect 1 | O75352 |
| C0020757 | Ichthyoses | MPDU1 | 9526 | mannose-P-dolichol utilization defect 1 | O75352 |
