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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	MIM:183090
Parent Relationships	is_a autosomal dominant cerebellar ataxia