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Summary Literature (0)
DOID:0060367 - Parkinson's disease 1

Disease Ontology Definition:A late onset Parkinson's disease that has_material_basis_in mutation in the alpha-synuclein gene on chromosome 4q22.1.

Synonyms: autosomal dominant Parkinson disease 1, autosomal dominant Parkinson's disease 1

Xenbase Genes : snca

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008200 - forehead

MIM:
MIM:168601 - PARKINSON DISEASE 1, AUTOSOMAL DOMINANT; PARK1

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)