| Approved symbol | OFD1 |
|---|---|
| Approved name | OFD1 centriole and centriolar satellite protein |
| HGCN ID | HGNC:2567 |
| Previous symbols | CXorf5, RP23 |
| Inheritance | |
| OMIM | 300170 |
| Chromosome | Xp22.2 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Epilepsy NGS Intellectual disability NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Primary ciliary dyskinesia PCD NGS Retinitis pigmentosa NGS Vision disorder CSNB |
