CHCHD2 deficiency

Synonym(s)
- Autosomal dominant Parkinson disease type 22
Type

Disease
External link(s)
- IEMbase
Gene
- CHCHD2 / Coiled-Coil-Helix-Coiled-Coil-Helix Domain Containing 2
  7p11.2
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Coiled-coil-helix-coiled-coil-helix domain-containing protein 2, mitochondrial
Disease group(s)
- 19.1 Disorders of mitochondrial membrane biogenesis and remodeling