/Parkinson disease 22, autosomal dominant

Parkinson disease 22, autosomal dominant

Rare Disease

MONDO:0014742

Also Known As

CHCHD2 Parkinson diseasePARK22Parkinson disease 22, autosomal dominantParkinson disease 22, autosomal dominant; PARK22Parkinson disease caused by mutation in CHCHD2

Definition

Any Parkinson disease in which the cause of the disease is a mutation in the CHCHD2 gene.

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Associated Genes

CHCHD2 ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:616710 ↗

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