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DOID 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

OMIM:615945

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is_a autosomal dominant cerebellar ataxia

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