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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 |
|---|---|---|---|---|---|
| C1261473 | Sarcoma | OGA | 10724 | O-GlcNAcase | O60502 |
| C0006826 | Malignant Neoplasms | OGA | 10724 | O-GlcNAcase | O60502 |
| C0037899 | Sphingolipidoses | OGA | 10724 | O-GlcNAcase | O60502 |
| C0752347 | Lewy Body Disease | OGA | 10724 | O-GlcNAcase | O60502 |
| C0751489 | Adult Sandhoff Disease | OGA | 10724 | O-GlcNAcase | O60502 |
| C1832916 | Timothy syndrome | OGA | 10724 | O-GlcNAcase | O60502 |
| C0026697 | Mucolipidoses | OGA | 10724 | O-GlcNAcase | O60502 |
| C0699790 | Colon Carcinoma | OGA | 10724 | O-GlcNAcase | O60502 |
| C0038868 | Progressive supranuclear palsy | OGA | 10724 | O-GlcNAcase | O60502 |
| C0233794 | Memory impairment | OGA | 10724 | O-GlcNAcase | O60502 |
| C0684249 | Carcinoma of lung | OGA | 10724 | O-GlcNAcase | O60502 |
| C0027765 | nervous system disorder | OGA | 10724 | O-GlcNAcase | O60502 |
| C0027051 | Myocardial Infarction | OGA | 10724 | O-GlcNAcase | O60502 |
| C0009319 | Colitis | OGA | 10724 | O-GlcNAcase | O60502 |
| C0017205 | Gaucher Disease | OGA | 10724 | O-GlcNAcase | O60502 |
| C1762616 | Meningioma, benign, no ICD-O subtype | OGA | 10724 | O-GlcNAcase | O60502 |
| C0011615 | Dermatitis, Atopic | OGA | 10724 | O-GlcNAcase | O60502 |
| C0041341 | Tuberous Sclerosis | OGA | 10724 | O-GlcNAcase | O60502 |
| C0268275 | Tay-Sachs Disease, AB Variant | OGA | 10724 | O-GlcNAcase | O60502 |
| C0002875 | Cooley's anemia | OGA | 10724 | O-GlcNAcase | O60502 |
| C0040517 | Gilles de la Tourette syndrome | OGA | 10724 | O-GlcNAcase | O60502 |
| C0007102 | Malignant tumor of colon | OGA | 10724 | O-GlcNAcase | O60502 |
| C0011854 | Diabetes Mellitus, Insulin-Dependent | OGA | 10724 | O-GlcNAcase | O60502 |
| C1832661 | ANOPHTHALMIA AND PULMONARY HYPOPLASIA | OGA | 10724 | O-GlcNAcase | O60502 |
| C4551898 | Cholestasis, progressive familial intrahepatic 1 | OGA | 10724 | O-GlcNAcase | O60502 |
