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Metadata
ID	DOID:0050985
Name	spinocerebellar ataxia type 38
Definition	An autosomal dominant cerebellar ataxia that is characterized by slowly progressive ataxia and nystagmus, presenting in mid-adulthood, and has_material_basis_in mutation to the ELOVL5 gene. https://www.omim.org/entry/615957
Xrefs	MIM:615957
Parent Relationships	is_a autosomal dominant cerebellar ataxia