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Metadata
ID	DOID:0050982
Name	spinocerebellar ataxia type 35
Definition	An autosomal dominant cerebellar ataxia that is characterized by a slowly progressive ataxia, tremor, dysarthria and hyperreflexia, has_material_basis_in mutation in the TGM6 gene. https://www.omim.org/entry/613908
Xrefs	OMIM:613908
Parent Relationships	is_a autosomal dominant cerebellar ataxia