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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 |
|---|---|---|---|---|---|
| C0020615 | Hypoglycemia | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0020538 | Hypertensive disease | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C1510502 | Oxyphilic Adenoma | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0020456 | Hyperglycemia | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0011854 | Diabetes Mellitus, Insulin-Dependent | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0019196 | Hepatitis C | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0028754 | Obesity | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0342276 | Maturity onset diabetes mellitus in young | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0025202 | melanoma | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C1857395 | De Toni-Debre-Fanconi Syndrome | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0027651 | Neoplasms | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C1565489 | Renal Insufficiency | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0021670 | insulinoma | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0013336 | Dwarfism | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C3887650 | Adult Rickets | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0268731 | Renal glomerular disease | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0025312 | Meningomyelocele | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C1833104 | DIABETES MELLITUS, PERMANENT NEONATAL | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0007102 | Malignant tumor of colon | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0015934 | Fetal Growth Retardation | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C1458155 | Mammary Neoplasms | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0268186 | Congenital glucose-galactose malabsorption | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0006826 | Malignant Neoplasms | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0085682 | Hypophosphatemia | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0007137 | Squamous cell carcinoma | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
