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Up to: Inborn organic aciduria · Glutaric aciduria
Glutaric acidemia type 3
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.
This condition has no sub-types.