| Term Name: | spinocerebellar ataxia 26 |
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| Synonyms: | |
| Definition: | An autosomal dominant cerebellar ataxia that is characterized by slowly progressive ataxia and oculomotor abnormalities, has_material_basis_in mutation in the EEF2 gene. |
| Ontology: | Human Disease [DOID:0050975] ( DOID:0050975 ) |