Classification of Inborn Errors of metabolism Medica DIsorders or amino acids Cystinuria Phenylketonuria Ty 们 sImi Homocyst fu na Non-ketonic hyperglycinemia Maple syrup urine disease Organic acidurias Isovaleric acidemia 3-methylcrotonmylCOA carboxylase deficiency 3 hylglutac。nic demia 3-hydroxy.3-methydgutaric acidemia Propionic acidemia MethyLmalonic academia Multiple carboxylase deficien Glutaric acidemia. type I Urea cycle defects Carbamoyl phosphate synthetase den ciency ornithine transcar amylase deficiency Citrul linemia Arginosuccinic aciduria Argininemia Lysinuric protein intolerance Sugar intolerances Classical galactosemia Galactokinase deficiency Epimerase deficiency Hereditary fructose intolerance Hereditary fructose-1.6 biphosphate se defICIEnCyMedical Genetics