| Approved symbol | ELOVL1 |
|---|---|
| Approved name | ELOVL fatty acid elongase 1 |
| HGCN ID | HGNC:14418 |
| Previous symbols | |
| Inheritance | |
| OMIM | 611813 |
| Chromosome | 1p34.2 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Retinitis pigmentosa NGS Treatable metabolic neurodegenerative disorders NGS Vision disorder CSNB |
