glutaric acidemia type 3 (DOID:0112246)
Alliance: disease page
Synonyms: GA3; GA III; glutaric aciduria 3; glutaric aciduria III; glutaric aciduria type 3; glutaryl-CoA oxidase deficiency
Alt IDs: OMIM:231690, ORDO:35706
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.