autosomal dominant cerebellar ataxia

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Summary

Literature (0)

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 Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: atxn10, tbp, itpr1, afg3l2, eef2

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): hereditary ataxia (is_a)