| E71 |
Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism |
| E71.0 |
Maple-syrup-urine disease |
| E71.1 |
Other disorders of branched-chain amino-acid metabolism |
| E71.11 |
Branched-chain organic acidurias |
| E71.110 |
Isovaleric acidemia |
| E71.111 |
3-methylglutaconic aciduria |
| E71.118 |
Other branched-chain organic acidurias |
| E71.12 |
Disorders of propionate metabolism |
| E71.120 |
Methylmalonic acidemia |
| E71.121 |
Propionic acidemia |
| E71.128 |
Other disorders of propionate metabolism |
| E71.19 |
Other disorders of branched-chain amino-acid metabolism |
| E71.2 |
Disorder of branched-chain amino-acid metabolism, unspecified |
| E71.3 |
Disorders of fatty-acid metabolism |
| E71.30 |
Disorder of fatty-acid metabolism, unspecified |
| E71.31 |
Disorders of fatty-acid oxidation |
| E71.310 |
Long chain/very long chain acyl CoA dehydrogenase deficiency |
| E71.311 |
Medium chain acyl CoA dehydrogenase deficiency |
| E71.312 |
Short chain acyl CoA dehydrogenase deficiency |
| E71.313 |
Glutaric aciduria type II |
| E71.314 |
Muscle carnitine palmitoyltransferase deficiency |
| E71.318 |
Other disorders of fatty-acid oxidation |
| E71.32 |
Disorders of ketone metabolism |
| E71.39 |
Other disorders of fatty-acid metabolism |
| E71.4 |
Disorders of carnitine metabolism |
| E71.40 |
Disorder of carnitine metabolism, unspecified |
| E71.41 |
Primary carnitine deficiency |
| E71.42 |
Carnitine deficiency due to inborn errors of metabolism |
| E71.43 |
Iatrogenic carnitine deficiency |
| E71.44 |
Other secondary carnitine deficiency |
| E71.440 |
Ruvalcaba-Myhre-Smith syndrome |
| E71.448 |
Other secondary carnitine deficiency |
| E71.5 |
Peroxisomal disorders |
| E71.50 |
Peroxisomal disorder, unspecified |
| E71.51 |
Disorders of peroxisome biogenesis |
| E71.510 |
Zellweger syndrome |
| E71.511 |
Neonatal adrenoleukodystrophy |
| E71.518 |
Other disorders of peroxisome biogenesis |
| E71.52 |
X-linked adrenoleukodystrophy |
| E71.520 |
Childhood cerebral X-linked adrenoleukodystrophy |
| E71.521 |
Adolescent X-linked adrenoleukodystrophy |
| E71.528 |
Other X-linked adrenoleukodystrophy |
| E71.529 |
X-linked adrenoleukodystrophy, unspecified type |
| E71.53 |
Other group 2 peroxisomal disorders |
| E71.54 |
Other peroxisomal disorders |
| E71.540 |
Rhizomelic chondrodysplasia punctata |
| E71.541 |
Zellweger-like syndrome |
| E71.542 |
Other group 3 peroxisomal disorders |
| E71.548 |
Other peroxisomal disorders |