OBO ID: DOID:0060897
Term Name: Parkinson's disease 17 Search Ontology:
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:
OTHER Parkinson's disease 17 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
VPS35 {Parkinson disease 17} 614203
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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