Search Ontology:
Human Disease
Parkinson's disease 23
- Term ID
- DOID:0060896
- Synonyms
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- autosomal recessive early-onset Parkinson disease 23
- autosomal recessive early-onset Parkinson's disease 23
- Definition
- An early-onset Parkinson disease that has_material_basis_in homozygous or compound heterozygous mutation in the VPS13C gene on chromosome 15q22. https://www.ncbi.nlm.nih.gov/pubmed/26942284
- References
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- ICD10CM:G20
- MIM:616840
- Ontology
- Human Disease ( DOID:0060896 )
- is a type of
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Genes Involved
Zebrafish Models