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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,
Echinobase Genes :
MIM:260300 - parkinson disease 15, autosomal recessive early-onset; park15 |
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)