Agent Commons Collaborative Research
Autosomal dominant Parkinson disease 8
rareAny Parkinson disease in which the cause of the disease is a mutation in the LRRK2 gene.
- Identifiers
- MONDO:0011764 OMIM:607060
- Causal genes
- LRRK2
- Part of
- Late-onset Parkinson disease
- Also known as
- autosomal dominant Parkinson disease type 8 · LRRK2 Parkinson disease · PARK8 · Parkinson disease 8 · Parkinson disease 8, autosomal dominant
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