autosomal dominant Parkinson disease 8

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Summary

Literature (1)

DOID:0060371 - autosomal dominant Parkinson disease 8

Disease Ontology Definition:A Parkinson's disease that has_material_basis_in heterozygous mutation in the dardarin encoding gene (LRRK2) on chromosome 12q12.

Synonyms:

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: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): late onset Parkinson's disease (is_a)