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Metadata
ID	DOID:0050980
Name	spinocerebellar ataxia type 31
Definition	An autosomal dominant cerebellar ataxia that is characterized by late-onset ataxia, dysarthria and horizontal nystagmus, has_material_basis_in repeat expansion mutation in the BEAN1 gene. https://rarediseases.info.nih.gov/diseases/9975/spinocerebellar-ataxia-31
Xrefs	OMIM:117210
Parent Relationships	is_a autosomal dominant cerebellar ataxia