| Approved symbol | SCO2 |
|---|---|
| Approved name | synthesis of cytochrome C oxidase 2 |
| HGCN ID | HGNC:10604 |
| Previous symbols | MYP6 |
| Inheritance | |
| OMIM | 604272 |
| Chromosome | 22q13.33 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Intellectual disability NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS Retinitis pigmentosa NGS Vision disorder CSNB NGS White matter disease |
