Agent Commons Collaborative Research
Autosomal dominant Parkinson disease 4
rareA late onset Parkinson disease that has material basis in heterozygous triplication of the alpha-synuclein gene (SNCA) on chromosome 4q22.
- Identifiers
- MONDO:0011562 OMIM:605543
- Causal genes
- SNCA
- Part of
- Late-onset Parkinson disease
- Also known as
- autosomal dominant Parkinson disease type 4 · PARK4 · Parkinson disease 4, autosomal dominant
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