FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term glutaric acidemia type 3 ID (Ontology) DOID:0112246 (Human Disease)
Definition A peroxisomal disease characterized by isolated accumulation of glutaric acid in the absence of other clinical phenotype that has_material_basis_in homozygous or compound heterozygous mutation in the SUGCT gene on chromosome 7p14.1.
Also Known As "GA III" ; "GA3" ; "glutaric aciduria 3" (for all, see Synonyms field below)
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 Genes
 glutaric acidemia type 3       1
 for disease ribbon | glutaric acidemia type 3       1
 model of | glutaric acidemia type 3       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
inherited metabolic disorder     |
 |__peroxisomal disease__________|
                                 glutaric acidemia type 3  1 rec.
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Is a autosomal recessive disease
peroxisomal disease
Part of
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Synonyms
  • "GA III" EXACT OMO:0003012
    "GA3" EXACT OMO:0003012
    "glutaric aciduria 3" EXACT
    "glutaric aciduria III" EXACT
    "glutaric aciduria type 3" EXACT
    "glutaryl-CoA oxidase deficiency" EXACT
Secondary IDs
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GARD:12469
MIM:231690
ORDO:35706