Category · E70-E88
E71Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
50 codes in this category
E71Disorders of branched-chain amino-acid metabolism and fatty-acid metabolismHeaderE71.0Maple-syrup-urine diseaseBillableE71.1Other disorders of branched-chain amino-acid metabolismHeaderE71.11Branched-chain organic aciduriasHeaderE71.110Isovaleric acidemiaBillableE71.1113-methylglutaconic aciduriaBillableE71.118Other branched-chain organic aciduriasBillableE71.12Disorders of propionate metabolismHeaderE71.120Methylmalonic acidemiaBillableE71.121Propionic acidemiaBillableE71.128Other disorders of propionate metabolismBillableE71.19Other disorders of branched-chain amino-acid metabolismBillableE71.2Disorder of branched-chain amino-acid metabolism, unspecifiedBillableE71.3Disorders of fatty-acid metabolismHeaderE71.30Disorder of fatty-acid metabolism, unspecifiedBillableE71.31Disorders of fatty-acid oxidationHeaderE71.310Long chain/very long chain acyl CoA dehydrogenase deficiencyBillableE71.311Medium chain acyl CoA dehydrogenase deficiencyBillableE71.312Short chain acyl CoA dehydrogenase deficiencyBillableE71.313Glutaric aciduria type IIBillableE71.314Muscle carnitine palmitoyltransferase deficiencyBillableE71.318Other disorders of fatty-acid oxidationBillableE71.32Disorders of ketone metabolismBillableE71.39Other disorders of fatty-acid metabolismBillableE71.4Disorders of carnitine metabolismHeaderE71.40Disorder of carnitine metabolism, unspecifiedBillableE71.41Primary carnitine deficiencyBillableE71.42Carnitine deficiency due to inborn errors of metabolismBillableE71.43Iatrogenic carnitine deficiencyBillableE71.44Other secondary carnitine deficiencyHeaderE71.440Ruvalcaba-Myhre-Smith syndromeBillableE71.448Other secondary carnitine deficiencyBillableE71.5Peroxisomal disordersHeaderE71.50Peroxisomal disorder, unspecifiedBillableE71.51Disorders of peroxisome biogenesisHeaderE71.510Zellweger syndromeBillableE71.511Neonatal adrenoleukodystrophyBillableE71.518Other disorders of peroxisome biogenesisBillableE71.52X-linked adrenoleukodystrophyHeaderE71.520Childhood cerebral X-linked adrenoleukodystrophyBillableE71.521Adolescent X-linked adrenoleukodystrophyBillableE71.522AdrenomyeloneuropathyBillableE71.528Other X-linked adrenoleukodystrophyBillableE71.529X-linked adrenoleukodystrophy, unspecified typeBillableE71.53Other group 2 peroxisomal disordersBillableE71.54Other peroxisomal disordersHeaderE71.540Rhizomelic chondrodysplasia punctataBillableE71.541Zellweger-like syndromeBillableE71.542Other group 3 peroxisomal disordersBillableE71.548Other peroxisomal disordersBillable