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DOID 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

OMIM:614153

Relationships

is_a autosomal dominant cerebellar ataxia

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