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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:
Echinobase Genes :
MIM:168601 - parkinson disease 1, autosomal dominant; park1 parkinson disease 1, autosomal dominant lewy body;; atypical parkinson disease, included |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
late onset Parkinson disease (is_a)