CHCHD2

coiled-coil-helix-coiled-coil-helix domain containing 2
OMIM: 616244
PanelMode of inheritanceDetails
1 panel
R-numbers: R58
Signed-off version 3.1
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Parkinson disease 22, autosomal dominant, OMIM:616710