FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term autosomal recessive spinocerebellar ataxia 2 ID (Ontology) DOID:0080061 (Human Disease)
Definition An autosomal recessive cerebellar ataxia that is characterized by juvenile onset of progressive cerebellar ataxia, axonal sensorimotor peripheral neuropathy, and increased serum alpha-fetoprotein, and has_material_basis_in homozygous or compound heterozygous mutation in the senataxin gene on chromosome 9q34.
Also Known As "SCAR2"
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 Genes
 autosomal recessive spinocerebellar ataxia 2       1
 for disease ribbon | autosomal recessive spinocerebellar ataxia 2       1
 model of | autosomal recessive spinocerebellar ataxia 2       1
Spanning Tree (Parents/Children)
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autosomal recessive disease__
cerebellar ataxia____________|
                             autosomal recessive cerebellar ataxia
                              |__autosomal recessive spinocerebellar ataxia 2  1 rec.
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Is a autosomal recessive cerebellar ataxia
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Synonyms
  • "SCAR2" EXACT OMO:0003012
Secondary IDs
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MIM:213200