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Human Disease

Parkinson's disease 17

Term ID
DOID:0060897
Synonyms
  • 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 )
Relationships
is a type of
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Genes Involved
Zebrafish Models