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DOID 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

OMIM:609306

Relationships

is_a autosomal dominant cerebellar ataxia

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