| Approved symbol | NYX |
|---|---|
| Approved name | nyctalopin |
| HGCN ID | HGNC:8082 |
| Previous symbols | CSNB1, CSNB4 |
| Inheritance | |
| OMIM | 300278 |
| Chromosome | Xp11.4 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Congenital stationary nightblindness NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Retinitis pigmentosa NGS Vision disorder CSNB NYX Analysis |
