Holocytochrome c synthase deficiency

Synonym(s)
- Linear skin defects with multiple congenital anomalies type 1
Type

Disease
External link(s)
- IEMbase
Gene
- HCCS / Holocytochrome C Synthase
  Xp22.2
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Holocytochrome C synthase
Disease group(s)
- 7.3 Disorders of nuclear encoded complex III subunits and assembly factors