Search Ontology:
Human Disease
Parkinson's disease 2
- Term ID
- DOID:0060368
- Synonyms
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- autosomal recessive juvenile Parkinson disease 2
- autosomal recessive juvenile Parkinson's disease 2
- Definition
- An early-onset Parkinson's disease that has_material_basis_in mutation in the parkin gene on chromosome 6q25.2-q27. https://www.ncbi.nlm.nih.gov/pubmed/22315721
- References
- Ontology
- Human Disease ( DOID:0060368 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models