Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition A rare inborn error of metabolism characterized by abnormally high urinary excretion of glutaric acid due to peroxisomal glutaryl-CoA oxidase deficiency. There is no association with a specific clinical phenotype. Disease data Classification Disease Synonyms Glutaric aciduria type 3 Acyduria glutarowa typu 3 Niedobór oksydazy glutarylo-CoA Glutaryl-CoA oxidase deficiency ORPHA code 35706 OMIM code 231690 ICD10 code E72.3 ICD11 code - *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl