Online 2016 ICD-10-CM · Tabular List · Alpha Index · ICD-9/ICD-10 conversion · ICD-10-PCS


 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
 E71.522 - Adrenomyeloneuropathy
 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