autosomal recessive spinocerebellar ataxia 15 Disease Ontology Browser

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Disease Ontology Browser

autosomal recessive spinocerebellar ataxia 15 (DOID:0080057)
Alliance: disease page
Synonyms: SCAR15
Alt IDs: OMIM:615705
Definition: An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous mutation in the RUBCN gene on chromosome 3q29.

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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