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 13 ID (Ontology) DOID:0080062 (Human Disease)
Definition An autosomal recessive cerebellar ataxia that is characterized by delayed psychomotor development beginning in infancy and that has_material_basis_in homozygous mutation in the GRM1 gene on chromosome 6q24.
Also Known As "SCAR13"
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Data Class Field Records
Human Disease Models (FBhh)  DOID       1
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 Genes Human Disease Models
 autosomal recessive spinocerebellar ataxia 13       1      1
 for disease ribbon | autosomal recessive spinocerebellar ataxia 13       1       --
 model of | autosomal recessive spinocerebellar ataxia 13       1       --
Spanning Tree (Parents/Children)
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autosomal recessive disease__
cerebellar ataxia____________|
                             autosomal recessive cerebellar ataxia
                              |__autosomal recessive spinocerebellar ataxia 13  2 rec.
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Is a autosomal recessive cerebellar ataxia
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Synonyms
  • "SCAR13" EXACT OMO:0003012
Secondary IDs
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MIM:614831