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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 ▼ |
|---|---|---|---|---|---|
| C0242363 | Islet Cell Tumor | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0016952 | Galactosemias | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0013595 | Eczema | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0524620 | Metabolic Syndrome X | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C1306459 | Primary malignant neoplasm | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0271708 | Fasting Hypoglycemia | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0011615 | Dermatitis, Atopic | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0001122 | Acidosis | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0007134 | Renal Cell Carcinoma | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0079731 | B-Cell Lymphomas | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0017980 | Glycosuria, Renal | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C3245525 | Familial renal glucosuria | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0010068 | Coronary heart disease | LIPC | 3990 | lipase C, hepatic type | P11150 |
| C1956346 | Coronary Artery Disease | LIPC | 3990 | lipase C, hepatic type | P11150 |
| C0028754 | Obesity | LIPC | 3990 | lipase C, hepatic type | P11150 |
| C0009402 | Colorectal Carcinoma | LIPC | 3990 | lipase C, hepatic type | P11150 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | LIPC | 3990 | lipase C, hepatic type | P11150 |
| C0036341 | Schizophrenia | LIPC | 3990 | lipase C, hepatic type | P11150 |
| C0745103 | Hyperlipoproteinemia Type IIa | LIPC | 3990 | lipase C, hepatic type | P11150 |
| C0019189 | Hepatitis, Chronic | LIPC | 3990 | lipase C, hepatic type | P11150 |
| C0342883 | Cholesteryl Ester Transfer Protein Deficiency | LIPC | 3990 | lipase C, hepatic type | P11150 |
| C0242383 | Age related macular degeneration | LIPC | 3990 | lipase C, hepatic type | P11150 |
| C0003850 | Arteriosclerosis | LIPC | 3990 | lipase C, hepatic type | P11150 |
| C0007222 | Cardiovascular Diseases | LIPC | 3990 | lipase C, hepatic type | P11150 |
| C0852036 | Pregnancy associated hypertension | LIPC | 3990 | lipase C, hepatic type | P11150 |
