spinocerebellar ataxia type 26

Term ID

DOID:0050975

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. https://rarediseases.info.nih.gov/diseases/9995/spinocerebellar-ataxia-26

References

• GARD:9995
• MESH:C537203
• OMIM:609306

Ontology

Human Disease   ( DOID:0050975 )