spinocerebellar ataxia type 18 Disease Ontology Browser

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Disease Ontology Browser

spinocerebellar ataxia type 18 (DOID:0050969)
Alliance: disease page
Alt IDs: OMIM:607458
Definition: An autosomal dominant cerebellar ataxia that is characterized by cerebellar ataxia and sensory neuropathy, has_material_basis_in mutation on chromosome 7q22-q23.

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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