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Disease Ontology Browser
spinocerebellar ataxia type 4 (DOID:0050957)
Alliance: disease page
Alt IDs: OMIM:600223, MESH:D020754, ORDO:98765, UMLS_CUI:C0752122
Definition: An autosomal dominant cerebellar ataxia that is characterized by progresive ataxia, dysarthria and peripheral neuropathy, has_material_basis_in mutation in the SCA4 gene.

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
04/23/2024
MGI 6.23 		The Jackson Laboratory