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Summary Literature (0)
DOID:0060897 - Parkinson's disease 17

Disease Ontology Definition:A late-onset Parkinson disease that has_material_basis_in heterozygous mutation in the VPS35 gene on chromosome 16q13.

Synonyms: autosomal dominant Parkinson disease 17, Parkinson disease 17

Xenbase Genes : vps35

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013625 - Parkinson disease 17

MIM:
MIM:614203 - PARKINSON DISEASE 17; PARK17

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), late onset Parkinson's disease (is_a)