Catalog

Glutaric aciduria type 3

No MMS code

Link to WHO Definition

Glutaric aciduria type 3 – http://id.who.int/icd/entity/627751573

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.