Parkinson's disease 14

Summary

DOID:0060900 - Parkinson's disease 14

Disease Ontology Definition:A late-onset Parkinson disease that has_material_basis_in homozygous mutation in the PLA2G6 gene on chromosome 22q13.

Synonyms: autosomal recessive Parkinson disease 14, autosomal recessive Parkinson's disease 14, Dystonia-Parkinsonism Adult-Onset

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

: pla2g6

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013060 - autosomal recessive Parkinson disease 14

MONDO:0013060 - autosomal recessive Parkinson disease 14

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), late onset Parkinson's disease (is_a)