Search Ontology:
Human Disease
GRID2-related spinocerebellar ataxia
- Term ID
- DOID:0050988
- Synonyms
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- Definition
- An autosomal dominant cerebellar ataxia that is characterized by cognitive delay, abnormal eye movements, and hearing loss. https://rarediseases.org/rare-diseases/autosomal-dominant-hereditary-ataxia/
- References
- Ontology
- Human Disease ( DOID:0050988 )
- is a type of
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