Parkinson's disease 2

Summary

DOID:0060368 - Parkinson's disease 2

Disease Ontology Definition:An early-onset Parkinson's disease that has_material_basis_in mutation in the parkin gene on chromosome 6q25.2-q27.

Synonyms: autosomal recessive juvenile Parkinson disease 2, autosomal recessive juvenile Parkinson's disease 2,

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

:

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010820 - autosomal recessive juvenile Parkinson disease 2

MONDO:0010820 - autosomal recessive juvenile Parkinson disease 2

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

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

Parent(s): autosomal recessive disease (is_a), early-onset Parkinson's disease (is_a), juvenile-onset Parkinson disease (is_a)