| 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 dystrophie en macula degeneratie NGS Intellectual disability NGS Leber congenital amaurosis LCA NGS Mendelioom NGS Preconceptiepanel (t.b.v. consanguine paren) NGS Retinitis pigmentosa NGS Visus pakket Retinale genen NGS Wittestofziekten |
