CHCHD2

coiled-coil-helix-coiled-coil-helix domain containing 2
OMIM: 616244, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green CHCHD2 in Early-onset Parkinson disease


Level 2: Neurology and neurodevelopmental disorders
Version 3.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Parkinson disease 22, autosomal dominant MIM#616710

Green CHCHD2 in Incidentalome


Version 1.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Parkinson disease 22, autosomal dominant MIM#616710
Tags
  • adult onset neurodegenerative

Green CHCHD2 in Mitochondrial disease


Level 2: Metabolic disorders
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Parkinson disease 22, autosomal dominant MIM#616710