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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](img/icons/info1.png)
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