Genomics England
GMS Panels
Panels
Genes and Entities
CHCHD2
coiled-coil-helix-coiled-coil-helix domain containing 2
OMIM:
616244
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Panel
Mode of inheritance
Details
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Adult onset neurodegenerative disorder
R-numbers:
R58
Signed-off version 6.6
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Parkinson disease 22, autosomal dominant, OMIM:616710