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Metadata
ID DOID:0050955
Name spinocerebellar ataxia type 2
Definition An autosomal dominant cerebellar ataxia that is characterized by ataxia, bulbar palsy, peripheral neuropathy chorea and muscle atrophy, has_material_basis_in mutation in the ATXN2 gene.
https://ghr.nlm.nih.gov/condition/spinocerebellar-ataxia-type-2
Xrefs

OMIM:183090

Parent Relationships

is_a autosomal dominant cerebellar ataxia

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