autosomal dominant cerebellar ataxia

Summary

DOID:1441 - autosomal dominant cerebellar ataxia

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

Synonyms: spinocerebellar ataxia

Xenbase 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

: fgf14, tbp, ifrd1, ttbk2, prkcg, atxn2, itpr1, afg3l2, ppp2r2b, elovl5, elovl4, atxn7, pum1, kcnc3, atxn10, [+]

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0020380 - autosomal dominant cerebellar ataxia

MONDO:0020380 - autosomal dominant cerebellar ataxia

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

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

Parent(s): autosomal dominant disease (is_a), cerebellar ataxia (is_a), hereditary ataxia (is_a)