| Approved symbol | CRX |
|---|---|
| Approved name | cone-rod homeobox |
| HGCN ID | HGNC:2383 |
| Previous symbols | CORD2 |
| Inheritance | |
| OMIM | 602225 |
| Chromosome | 19q13.33 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Retinitis pigmentosa NGS Vision disorder CSNB |
