Search Ontology:
Human Disease
GRID2-related spinocerebellar ataxia
- Term ID
- DOID:0050988
- 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 )
- is a type of
-
Show first 5 Terms
Other Pages
Genes Involved
Zebrafish Models
Citations