Search Ontology:
Human Disease
Parkinson's disease 8
- Term ID
- DOID:0060371
- Synonyms
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- autosomal dominant Parkinson disease 8
- autosomal dominant Parkinson's disease 8
- Definition
- A late onset Parkinson's disease that has_material_basis_in heterozygous mutation in the dardarin encoding gene on chromosome 12q12. https://www.ncbi.nlm.nih.gov/pubmed/22315721
- References
- Ontology
- Human Disease ( DOID:0060371 )
- is a type of
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