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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 ▲ |
|---|---|---|---|---|---|
| C1306459 | Primary malignant neoplasm | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
| C0162429 | Malnutrition | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
| C0020473 | Hyperlipidemia | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
| C0220981 | Metabolic acidosis | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
| C0030305 | Pancreatitis | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
| C0017638 | Glioma | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
| C0029438 | Massive Osteolyses | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
| C2919796 | Glycogen storage disease type Ia | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
| C0011847 | Diabetes | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
| C0006826 | Malignant Neoplasms | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
| C0011854 | Diabetes Mellitus, Insulin-Dependent | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
| C0740394 | Hyperuricemia | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
| C0020538 | Hypertensive disease | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
| C0271708 | Fasting Hypoglycemia | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
| C0033687 | Proteinuria | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
| C0020615 | Hypoglycemia | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
| C0018099 | Gout | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
| C0043325 | Xanthomatosis | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
| C1621958 | Glioblastoma Multiforme | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
| C0038644 | Sudden infant death syndrome | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
| C0029456 | Osteoporosis | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
| C3203102 | Idiopathic pulmonary arterial hypertension | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
| C0149745 | Oral Ulcer | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
| C0302314 | Xanthoma | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
| C0022658 | Kidney Diseases | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
