GRID2-related spinocerebellar ataxia Disease Ontology Browser

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Disease Ontology Browser

GRID2-related spinocerebellar ataxia (DOID:0050988)
Alliance: disease page
Definition: An autosomal dominant cerebellar ataxia that is characterized by cognitive delay, abnormal eye movements, and hearing loss.

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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