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Summary Literature (1)
DOID:1441 - autosomal dominant cerebellar ataxia


Disease Ontology Definition:A hereditary ataxia that has_material_basis_in autosomal dominant inheritance.

Synonyms: spinocerebellar ataxia

Referenced OMIM:

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : fgf14, tbp, ttbk2, prkcg, atxn2, itpr1, afg3l2, ppp2r2b, atxn7, kcnc3, atxn10, eef2.1, atxn3, atxn1, sptbn2, [+]

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): hereditary ataxia (is_a)


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