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DOID:1441 - autosomal dominant cerebellar ataxia
Disease Ontology Definition:A hereditary ataxia that has_material_basis_in autosomal dominant inheritance.
Synonyms: spinocerebellar ataxia ,
Echinobase Genes : atxn10, tbp, itpr1, afg3l2, eef2
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
hereditary ataxia (is_a)