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E71.2 Disorder of branched-chain amino-acid metabolism, unspecified
- E71.3 Disorders of fatty-acid metabolism
- Excludes1: peroxisomal disorders (E71.5)
- Refsum's disease (G60.1)
- Schilder's disease (G37.0)
- Excludes2: carnitine deficiency due to inborn error of metabolism (E71.42)
- 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
- LCAD
- VLCAD
- E71.311 Medium chain acyl CoA dehydrogenase deficiency
- MCAD
- E71.312 Short chain acyl CoA dehydrogenase deficiency
- SCAD
- E71.313 Glutaric aciduria type II
- Glutaric aciduria type II A
- Glutaric aciduria type II B
- Glutaric aciduria type II C
- Excludes1: glutaric aciduria (type 1) NOS (E72.3)
- E71.314 Muscle carnitine palmitoyltransferase deficiency
- E71.318 Other disorders of fatty-acid oxidation
- E71.310 Long chain/very long chain acyl CoA dehydrogenase deficiency
- E71.32 Disorders of ketone metabolism
- E71.39 Other disorders of fatty-acid metabolism
- Excludes1: peroxisomal disorders (E71.5)
- E71.4 Disorders of carnitine metabolism
- Excludes1: Muscle carnitine palmitoyltransferase deficiency (E71.314)
- E71.40 Disorder of carnitine metabolism, unspecified
- E71.41 Primary carnitine deficiency
- E71.42 Carnitine deficiency due to inborn errors of metabolism
- Code also associated inborn error or metabolism
- E71.43 Iatrogenic carnitine deficiency
- Carnitine deficiency due to:
- hemodialysis
- Valproic acid therapy
- E71.44 Other secondary carnitine deficiency
- E71.440 Ruvalcaba-Myhre-Smith syndrome
- E71.448 Other secondary carnitine deficiency
- E71.5 Peroxisomal disorders
- Excludes1: Schilder?s disease (G37.0)
- E71.50 Peroxisomal disorder, unspecified
- E71.