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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 |
|---|---|---|---|---|---|
| C0035222 | Respiratory Distress Syndrome, Adult | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
| C0022283 | Incontinentia Pigmenti Achromians | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
| C0524620 | Metabolic Syndrome X | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
| C1332206 | Adult Lymphoma | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
| C0006267 | Bronchiectasis | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
| C0340076 | Asthmatic pulmonary eosinophilia | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
| C0023890 | Liver Cirrhosis | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
| C1306459 | Primary malignant neoplasm | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
| C0751606 | Adult Acute Lymphocytic Leukemia | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
| C0034068 | Pulmonary Eosinophilia | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
| C0162309 | Adrenoleukodystrophy | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
| C0023467 | Leukemia, Myelocytic, Acute | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
| C1850900 | Familial primary gastric lymphoma | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
| C0028754 | Obesity | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
| C0162557 | Liver Failure, Acute | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
| C0023452 | Childhood Acute Lymphoblastic Leukemia | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
| C0279626 | Squamous cell carcinoma of esophagus | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
| C0023449 | Acute lymphocytic leukemia | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
| C1847593 | EPIPHYSEAL DYSPLASIA, MULTIPLE, 4 | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C1850555 | De La Chapelle Dysplasia | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0265274 | Achondrogenesis, type IB (disorder) | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C1384666 | hearing impairment | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C1850554 | Atelosteogenesis type 2 | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0220726 | Diastrophic dysplasia | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0029422 | Osteochondrodysplasias | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
