FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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Term spinocerebellar ataxia type 36 ID (Ontology) DOID:0050983 (Human Disease)
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.
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 spinocerebellar ataxia type 36       1
 for disease ribbon | spinocerebellar ataxia type 36       1
 model of | spinocerebellar ataxia type 36       1
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autosomal dominant disease__
cerebellar ataxia___________|
                            autosomal dominant cerebellar ataxia
                             |__spinocerebellar ataxia type 36  1 rec.
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Is a autosomal dominant cerebellar ataxia
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MIM:614153