Codes Related to ICD-10 E71.32

Disorders of ketone metabolism

ICD-10 Related Codes to E71.32

  • 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
  • E71.39 - 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
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