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Metadata
ID	DOID:0050983
Name	spinocerebellar ataxia type 36
Definition	An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, dysarthria, hyperreflexia, sensiorineural hearing loss and muscle atrophy, has_material_basis_in mutation in the NOP56 gene. https://ghr.nlm.nih.gov/condition/spinocerebellar-ataxia-type-36
Xrefs	MIM:614153
Parent Relationships	is_a autosomal dominant cerebellar ataxia