Parkinson's disease 8

Summary

DOID:0060371 - Parkinson's disease 8

Disease Ontology Definition:A late onset Parkinson's disease that has_material_basis_in heterozygous mutation in the dardarin encoding gene on chromosome 12q12.

Synonyms: autosomal dominant Parkinson disease 8, autosomal dominant Parkinson's disease 8

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

: lrrk2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011764 - autosomal dominant Parkinson disease 8

MONDO:0011764 - autosomal dominant Parkinson disease 8

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)