| Metadata | |
|---|---|
| ID | DOID:0050988 |
| Name | GRID2-related spinocerebellar ataxia |
| 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/ |
| Parent Relationships |