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Disease Ontology Browser
autosomal dominant cerebellar ataxia (DOID:1441)
Alliance: disease page
Synonyms: spinocerebellar ataxia
Alt IDs: DOID:2478, ICD9CM:334.3, MESH:D020754, NCI:C82341, OMIM:PS164400, ORDO:94, UMLS_CUI:C0087012
Definition: A cerebellar ataxia that has_material_basis_in autosomal dominant inheritance.

Disease References using Mouse Models (82)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory