autosomal recessive spinocerebellar ataxia 10 Disease Ontology Browser

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Disease Ontology Browser

autosomal recessive spinocerebellar ataxia 10 (DOID:0050999)
Alliance: disease page
Synonyms: SCAR10
Alt IDs: OMIM:613728
Definition: An autosomal recessive cerebellar ataxia that is characterized by ataxia, dysarthria, nystagmus and marked cerebellar atrophy, has_material_basis_in mutation in the ANO10 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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