FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term spinocerebellar ataxia type 37 ID (Ontology) DOID:0050984 (Human Disease)
Definition An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia and dysarthria, presenting in mid-adulthood, and has_material_basis_in mutation to the DAB1 gene.
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 spinocerebellar ataxia type 37       1
 for disease ribbon | spinocerebellar ataxia type 37       1
 model of | spinocerebellar ataxia type 37       1
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autosomal dominant disease__
cerebellar ataxia___________|
                            autosomal dominant cerebellar ataxia
                             |__spinocerebellar ataxia type 37  1 rec.
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Is a autosomal dominant cerebellar ataxia
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MIM:615945