Glutaric acidemia type 3

MONDO:0009283

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.

Also known as: SUGCT glutaric aciduria (disease), glutaric acidemia type 3, glutaric aciduria (disease) caused by mutation in SUGCT, glutaric aciduria type 3, glutaryl-CoA oxidase deficiency, GA III, GA3, Ga 3

0 clinical trials for this condition and its sub-types, 0 tagged with Glutaric acidemia type 3 itself.

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↑ Inborn organic aciduria (29) ↑ Glutaric aciduria (5)

Including sub-types (0) Tagged with Glutaric acidemia type 3 (0)

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