OBO ID: DOID:0050988
Term Name: GRID2-related spinocerebellar ataxia Search Ontology:
Synonyms:
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 )
Relationships
is a type of:
OTHER GRID2-related spinocerebellar ataxia PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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