| Approved symbol | ACBD5 |
|---|---|
| Approved name | acyl-CoA binding domain containing 5 |
| HGCN ID | HGNC:23338 |
| Previous symbols | |
| Inheritance | |
| OMIM | 616618 |
| Chromosome | 10p12.1 |
| 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 |
