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Namespace Prefixes

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Statements

Subject Item

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An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, dysarthria, hyperreflexia, ophthalmoparesis, nystagmus and ptosis, and has_material_basis_in mutation in the AFG3L2 gene.

obo:hasDbXref

url:https://rarediseases.info.nih.gov/diseases/9951/spinocerebellar-ataxia-28