| Approved symbol | LCA5 |
|---|---|
| Approved name | lebercilin LCA5 |
| HGCN ID | HGNC:31923 |
| Previous symbols | C6orf152 |
| Inheritance | |
| OMIM | 611408 |
| Chromosome | 6q14.1 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS Retinitis pigmentosa NGS Vision disorder CSNB |
