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Metadata
ID	DOID:0050984
Name	spinocerebellar ataxia type 37
Definition	An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia and dysarthria, presenting in mid-adulthood, and has_material_basis_in mutation to the DAB1 gene. https://www.omim.org/entry/615945
Xrefs	MIM:615945
Parent Relationships	is_a autosomal dominant cerebellar ataxia