Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (1)
DOID:1441 - autosomal dominant cerebellar ataxia

Disease Ontology Definition:A cerebellar 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, pum1, kcnc3, atxn10, eef2.1, atxn3, atxn1, [+]

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

Xenbase: The Xenopus Model Organism Knowledgebase.
Version: 4.15.0
Major funding for Xenbase is provided by grant P41 HD064556