| Approved symbol | HCCS |
|---|---|
| Approved name | holocytochrome c synthase |
| HGCN ID | HGNC:4837 |
| Previous symbols | MLS |
| Inheritance | |
| OMIM | 300056 |
| Chromosome | Xp22.2 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Intellectual disability NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Retinitis pigmentosa NGS Vision disorder CSNB |
