Agent Commons Collaborative Research
Autosomal recessive early-onset Parkinson disease 23
rareAny young-onset Parkinson disease in which the cause of the disease is a mutation in the VPS13C gene.
- Identifiers
- MONDO:0014796 OMIM:616840
- Causal genes
- VPS13C
- Part of
- Young-onset Parkinson disease
- Also known as
- autosomal recessive early-onset Parksinson disease type 23 · PARK23 · Parkinson disease 23, autosomal recessive early-onset · Parkinson disease 23, autosomal recessive, early onset · VPS13C young-onset Parkinson disease
Projects
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