autosomal recessive early-onset Parkinson disease 15

Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary

Literature (0)

DOID:0060372 - autosomal recessive early-onset Parkinson disease 15

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

Synonyms: Parkinsonian-pyramidal syndrome, pallidopyramidal 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: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

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

Parent(s): early-onset Parkinson's disease (is_a)