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Human Disease
Parkinson's disease 22
- Term ID
- DOID:0080504
- Synonyms
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- autosomal dominant Parkinson's disease 22
- Definition
- A late onset Parkinson's disease that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the coiled-coil-helix-coiled-coil-helix domain containing 2 gene on chromosome 7p11.2. (2)
- References
- Ontology
- Human Disease ( DOID:0080504 )
- is a type of
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