| Approved symbol | CYP4V2 |
|---|---|
| Approved name | cytochrome P450 family 4 subfamily V member 2 |
| HGCN ID | HGNC:23198 |
| Previous symbols | |
| Inheritance | |
| OMIM | 608614 |
| Chromosome | 4q35.1-q35.2 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Congenital stationary nightblindness NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS Retinitis pigmentosa NGS Vision disorder CSNB |
