/glutaric acidemia type 3

glutaric acidemia type 3

Rare Disease

MONDO:0009283

Also Known As

SUGCT glutaric aciduria (disease)glutaric acidemia type 3glutaric aciduria (disease) caused by mutation in SUGCTglutaric aciduria type 3glutaryl-CoA oxidase deficiencyGA IIIGA3Ga 3glutaric acidemia type IIIglutaric aciduria 3glutaric aciduria IIIglutaric aciduria type IIIglutaryl-Coa oxidase deficiency

Definition

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.