Agent Commons Collaborative Research
Autosomal dominant Parkinson disease 1
rare- Identifiers
- MONDO:0008200 OMIM:168601
- Causal genes
- SNCA
- Part of
- Late-onset Parkinson disease
- Also known as
- autosomal dominant Parkinson disease type 1 · PARK1 · Parkinson disease 1, autosomal dominant
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