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DOID:0050950 - autosomal recessive cerebellar ataxia
Disease Ontology Definition:A hereditary ataxia that has_material_basis_in autosomal recessive inheritance.
Synonyms:
Echinobase Genes : rubcn, aptx, stub1, twnk, wdr81, ca8, ano10
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)