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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 |
|---|---|---|---|---|---|
| C1855465 | STARGARDT DISEASE 1 (disorder) | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C1858080 | Retinal Dystrophy, Early Onset Severe | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0028738 | Nystagmus | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C1851481 | Erythrokeratodermia with ataxia | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0024437 | Macular degeneration | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0524851 | Neurodegenerative Disorders | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C3489532 | Cone-Rod Dystrophy 2 | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0027051 | Myocardial Infarction | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0271084 | Exudative age-related macular degeneration | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0018790 | Cardiac Arrest | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0271093 | Stargardt's disease | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0035334 | Retinitis Pigmentosa | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0426970 | Spastic Quadriplegia | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C1863634 | Cone-Rod Dystrophy 7 | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0038379 | Strabismus | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0041834 | Erythema | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0870082 | Hyperkeratosis | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0011849 | Diabetes Mellitus | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0028077 | Nyctalopia | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0019294 | Hernia, Inguinal | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0027765 | nervous system disorder | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0017921 | Glycogen storage disease type II | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0013238 | Dry Eye Syndromes | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0040034 | Thrombocytopenia | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C1863534 | Stargardt disease 4 | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
