Glutaryl-CoA oxidase deficiency is a peroxisomal disorder leading to glutaric aciduria. The prevalence is unknown. There is no distinctive phenotype associated with this disorder and one of the reported cases was asymptomatic. Transmission appears to be autosomal recessive. The disease is glutaric acidemia type 3 (Monarch Disease Ontology entry MONDO_0009283). Also known as: SUGCT glutaric aciduria (disease), glutaric aciduria (disease) caused by mutation in SUGCT, glutaric aciduria type 3, glutaryl-CoA oxidase deficiency.