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 31 ID (Ontology) DOID:0070412 (Human Disease)
Definition An autosomal recessive cerebellar ataxia characterized by global developmental delay with hypotonia and variably impaired intellectual and language development that has_material_basis_in homozygous or compound heterozygous mutation in the ATG7 gene on chromosome 3p25.
Also Known As "SCAR31"
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 Genes
 autosomal recessive spinocerebellar ataxia 31       1
 for disease ribbon | autosomal recessive spinocerebellar ataxia 31       1
 model of | autosomal recessive spinocerebellar ataxia 31       1
Spanning Tree (Parents/Children)
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autosomal recessive disease__
cerebellar ataxia____________|
                             autosomal recessive cerebellar ataxia
                              |__autosomal recessive spinocerebellar ataxia 31  1 rec.
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Is a autosomal recessive cerebellar ataxia
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Synonyms
  • "SCAR31" EXACT OMO:0003012
Secondary IDs
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MIM:619422