Search Ontology:
Human Disease
Parkinson's disease 17
- Term ID
- DOID:0060897
- Synonyms
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- autosomal dominant Parkinson disease 17
- Parkinson disease 17
- Definition
- A late-onset Parkinson disease that has_material_basis_in heterozygous mutation in the VPS35 gene on chromosome 16q13. https://www.ncbi.nlm.nih.gov/pubmed/21763483
- References
- Ontology
- Human Disease ( DOID:0060897 )
- is a type of
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