Parkinson disease 22, autosomal dominant

Definition

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 — per MONDO

Also identified as

• DOID 0080504 per MONDO
• OMIM 616710 per MONDO
• UMLS C4225238 per MONDO