has material basis in germline mutation in SUGCT glutaric aciduria inborn organic aciduria glutaric acidemia type 3 https://github.com/monarch-initiative/mondo/issues/4985 https://rarediseases.info.nih.gov/diseases/12469/glutaric-acidemia-type-iii https://www.malacards.org/card/glutaric_aciduria_iii 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. GA3 DOID:0112246 MESH:C562818 GARD:0012469 Orphanet:35706 glutaric aciduria (disease) caused by mutation in SUGCT UMLS:C0342873 MEDGEN:87464 glutaryl-CoA oxidase deficiency SCTID:238070003 SUGCT glutaric aciduria (disease) glutaric aciduria type 3 GA III glutaric acidemia type 3 ICD9:270.2 glutaric acidemia type III glutaric aciduria type III OMIM:231690 obsolete disorder of peroxisomal alpha-, beta- and omega-oxidation