Parkinson's disease 15

Summary

DOID:0060372 - Parkinson's disease 15

Disease Ontology Definition:An early-onset Parkinson's disease that has_material_basis_in mutation in the FBXO7 gene on chromosome 22q12.3.

Synonyms: autosomal recessive early-onset Parkinson disease 15, autosomal recessive early-onset Parkinson's disease 15, pallidopyramidal syndrome, Parkinsonian-pyramidal syndrome

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

: fbxo7, snca

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0009830 - parkinsonian-pyramidal syndrome

MONDO:0009830 - parkinsonian-pyramidal syndrome

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)