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Human Disease

spinocerebellar ataxia type 31

Term ID
DOID:0050980
Synonyms
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
References
Ontology
Human Disease   ( DOID:0050980 )
Relationships
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Genes Involved
Zebrafish Models