Parkinson's disease 23

Summary

DOID:0060896 - Parkinson's disease 23

Disease Ontology Definition:An early-onset Parkinson disease that has_material_basis_in homozygous or compound heterozygous mutation in the VPS13C gene on chromosome 15q22.

Synonyms: autosomal recessive early-onset Parkinson disease 23, autosomal recessive early-onset Parkinson's disease 23

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

: vps13c

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014796 - autosomal recessive early-onset Parkinson disease 23

MONDO:0014796 - autosomal recessive early-onset Parkinson disease 23

Other Model Organisms: Alliance, 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)