Parkinson disease 22, autosomal dominant

MONDO:0014742

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

Also known as: CHCHD2 Parkinson disease, PARK22, Parkinson disease 22, autosomal dominant, Parkinson disease 22, autosomal dominant; PARK22, Parkinson disease caused by mutation in CHCHD2

12 clinical trials for this condition and its sub-types, 0 tagged with Parkinson disease 22, autosomal dominant itself.

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Part of

↑ Late-onset Parkinson disease (143)

Including sub-types (12) Tagged with Parkinson disease 22, autosomal dominant (0)

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