E712026
Non-billableDisorders of branched-chain amino-acid metabolism and fatty-acid metabolism
Clinical Notes
FAQ
Related Codes
E71Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
E71.0Maple-syrup-urine disease
E71.1Other disorders of branched-chain amino-acid metabolism
E71.11Branched-chain organic acidurias
E71.110Isovaleric acidemia
E71.1113-methylglutaconic aciduria
E71.118Other branched-chain organic acidurias
E71.12Disorders of propionate metabolism
E71.120Methylmalonic acidemia
E71.121Propionic acidemia
E71.128Other disorders of propionate metabolism
E71.19Other disorders of branched-chain amino-acid metabolism
E71.2Disorder of branched-chain amino-acid metabolism, unspecified
E71.3Disorders of fatty-acid metabolism
E71.30Disorder of fatty-acid metabolism, unspecified
E71.31Disorders of fatty-acid oxidation
E71.310Long chain/very long chain acyl CoA dehydrogenase deficiency
E71.311Medium chain acyl CoA dehydrogenase deficiency
E71.312Short chain acyl CoA dehydrogenase deficiency
E71.313Glutaric aciduria type II
E71.314Muscle carnitine palmitoyltransferase deficiency
E71.318Other disorders of fatty-acid oxidation
E71.32Disorders of ketone metabolism
E71.39Other disorders of fatty-acid metabolism
E71.4Disorders of carnitine metabolism
E71.40Disorder of carnitine metabolism, unspecified
E71.41Primary carnitine deficiency
E71.42Carnitine deficiency due to inborn errors of metabolism
E71.43Iatrogenic carnitine deficiency
E71.44Other secondary carnitine deficiency
E71.440Ruvalcaba-Myhre-Smith syndrome
E71.448deficiency
E71.5Peroxisomal disorders
E71.50Peroxisomal disorder, unspecified
E71.51Disorders of peroxisome biogenesis
E71.510Zellweger syndrome
E71.511Neonatal adrenoleukodystrophy
E71.518Other disorders of peroxisome biogenesis
E71.52X-linked adrenoleukodystrophy
E71.520Childhood cerebral X-linked adrenoleukodystrophy
E71.521Adolescent X-linked adrenoleukodystrophy
E71.522Adrenomyeloneuropathy
E71.528Other X-linked adrenoleukodystrophy
E71.529unspecified type
E71.53Other group 2 peroxisomal disorders
E71.54Other peroxisomal disorders
E71.540Rhizomelic chondrodysplasia punctata
E71.541Zellweger-like syndrome
E71.542Other group 3 peroxisomal disorders
E71.548Other peroxisomal disorders
Related Categories
E70Disorders of aromatic amino-acid metabolismE72Other disorders of amino-acid metabolismE73Lactose intoleranceE74Other disorders of carbohydrate metabolismE75Disorders of sphingolipid metabolism and other lipid storage disordersE76Disorders of glycosaminoglycan metabolismE77Disorders of glycoprotein metabolismE78Disorders of lipoprotein metabolism and other lipidemiasE79Disorders of purine and pyrimidine metabolismE80Disorders of porphyrin and bilirubin metabolismE83Disorders of mineral metabolismE84Cystic fibrosisE85AmyloidosisE86Volume depletionE87Other disorders of fluid, electrolyte and acid-base balanceE88Other and unspecified metabolic disorders