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Metadata
ID	DOID:0050979
Name	spinocerebellar ataxia type 30
Definition	An autosomal dominant cerebellar ataxia that is characterized by slowly progressive gait abnormalities and dysarthria, has_material_basis_in mutation in the ODZ3 gene. https://www.omim.org/entry/613371
Xrefs	GARD:4950 OMIM:613371
Subsets	DO_rare_slim
Parent Relationships	is_a autosomal dominant cerebellar ataxia