Term Name:	glutaric acidemia type 3
Synonyms:	GA III, GA3, glutaric aciduria 3, glutaric aciduria III, glutaric aciduria type 3, glutaryl-CoA oxidase deficiency
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.
Ontology:	Human Disease [DOID:0112246]   ( DOID:0112246 )