Parkinson's disease 4

Summary

DOID:0060895 - Parkinson's disease 4

Disease Ontology Definition:A late onset Parkinson disease that has_material_basis_in heterozygous triplication of the alpha-synuclein gene on chromosome 4q22.

Synonyms: autosomal dominant Lewy body Parkinson disease 4, autosomal dominant Parkinson disease 4, autosomal dominant Parkinson's disease 4

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: snca

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011562 - autosomal dominant Parkinson disease 4

MONDO:0011562 - autosomal dominant Parkinson disease 4

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)