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Metadata
ID	DOID:0050975
Name	spinocerebellar ataxia type 26
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. https://rarediseases.info.nih.gov/diseases/9995/spinocerebellar-ataxia-26
Xrefs	GARD:9995 MESH:C537203 MIM:609306
Subsets	DO_rare_slim
Parent Relationships	is_a autosomal dominant cerebellar ataxia