| E71 | Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism |
| | Maple-syrup-urine disease |
| | Other disorders of branched-chain amino-acid metabolism |
| | Branched-chain organic acidurias |
| | Isovaleric acidemia |
| | 3-methylglutaconic aciduria |
| | Other branched-chain organic acidurias |
| | Disorders of propionate metabolism |
| | Methylmalonic acidemia |
| | Propionic acidemia |
| | Other disorders of propionate metabolism |
| | Other disorders of branched-chain amino-acid metabolism |
| | Disorder of branched-chain amino-acid metabolism, unspecified |
| | Disorders of fatty-acid metabolism |
| | Disorder of fatty-acid metabolism, unspecified |
| | Disorders of fatty-acid oxidation |
| | Long chain/very long chain acyl CoA dehydrogenase deficiency |
| | Medium chain acyl CoA dehydrogenase deficiency |
| | Short chain acyl CoA dehydrogenase deficiency |
| | Glutaric aciduria type II |
| | Muscle carnitine palmitoyltransferase deficiency |
| | Other disorders of fatty-acid oxidation |
| | Disorders of ketone metabolism |
| | Other disorders of fatty-acid metabolism |
| | Disorders of carnitine metabolism |
| | Disorder of carnitine metabolism, unspecified |
| | Primary carnitine deficiency |
| | Carnitine deficiency due to inborn errors of metabolism |
| | Iatrogenic carnitine deficiency |
| | Other secondary carnitine deficiency |
| | Ruvalcaba-Myhre-Smith syndrome |
| | Other secondary carnitine deficiency |
| | Peroxisomal disorders |
| | Peroxisomal disorder, unspecified |
| | Disorders of peroxisome biogenesis |
| | Zellweger syndrome |
| | Neonatal adrenoleukodystrophy |
| | Other disorders of peroxisome biogenesis |
| | X-linked adrenoleukodystrophy |
| | Childhood cerebral X-linked adrenoleukodystrophy |
| | Adolescent X-linked adrenoleukodystrophy |
| | Adrenomyeloneuropathy |
| | Other X-linked adrenoleukodystrophy |
| | X-linked adrenoleukodystrophy, unspecified type |
| | Other group 2 peroxisomal disorders |
| | Other peroxisomal disorders |
| | Rhizomelic chondrodysplasia punctata |
| | Zellweger-like syndrome |
| | Other group 3 peroxisomal disorders |
| | Other peroxisomal disorders |
