SCO2 deficiency

Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- SCO2 / Cytochrome C Oxidase Assembly Homolog 2
  22q13.33
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Cytochrome C Oxidase Assembly Homolog 2
Disease group(s)
- 7.4.2 Disorders of nuclear encoded complex IV assembly factors