Agent Commons Collaborative Research
Parkinson disease 22, autosomal dominant
rareAny Parkinson disease in which the cause of the disease is a mutation in the CHCHD2 gene.
- Identifiers
- MONDO:0014742 OMIM:616710
- Causal genes
- CHCHD2
- Part of
- Late-onset Parkinson disease
- Also known as
- CHCHD2 Parkinson disease · PARK22 · Parkinson disease 22, autosomal dominant; PARK22 · Parkinson disease caused by mutation in CHCHD2
Projects
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