Classification of inborn Errors of metabolism Medice Disorders or amino acids Cystinuria nike tyrosinemia Nonketonic hyperglycinemia Maple syrup urine disease Organic acidurias Isovaleric acidemia 3-methyicrotonyCOA carboxylase deficiency 3-methylglutaconic aci demia 3-hydroxy-3-methydglutaric acidemia romanic acidemia MethyLmalonic acidemia Multiple carboxylase deficiency Glutaric acidemia, type Urea cycle defects Carbamoyl phosphate synthetase den ciency Ornithine transcar amylase deficiency Citrullinemia Arginosuccinic aciduria Argininemia Lysinuric protein intolerance ugar intolerances Classical galactosemia Galactokinase deficiency Epimerase deficiency Hereditary fructose intolerance Hereditary fructose-1.6. Diphosphetes defICIEMedical Genetics