| 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 Skeletal Dysplasia NGS Vision disorder CSNB |
