|
DOID:0060367 - autosomal dominant Parkinson disease 1
Disease Ontology Definition:A Parkinson's disease that has_material_basis_in mutation in the alpha-synuclein (SNCA) gene on chromosome 4q22.1.
Synonyms:
Xenbase Genes : snca
MONDO:0008200 - autosomal dominant Parkinson disease 1 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
late onset Parkinson's disease (is_a)