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E71.310

Long chain/very long chain acyl CoA dehydrogenase deficiency

Instruction Source: E71.310

Long chain/very long chain acyl CoA dehydrogenase deficiency

Instruction Source: E71.31

Disorders of fatty-acid oxidation

Instruction Source: E71.3

Disorders of fatty-acid metabolism

Excludes 1 (Mutually Exclusive)

  • Refsum's disease (G60.1)
  • Schilder's disease (G37.0)
  • peroxisomal disorders (E71.5)

Excludes 2 (Not Included Here)

  • carnitine deficiency due to inborn error of metabolism (E71.42)
Instruction Source: E71

Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism

Instruction Source: E70-E88

Metabolic disorders (E70-E88)

Excludes 1 (Mutually Exclusive)

  • 5-alpha-reductase deficiency (E29.1)
  • Marfan syndrome (Q87.4-)
  • androgen insensitivity syndrome (E34.5-)
  • congenital adrenal hyperplasia (E25.0)
  • hemolytic anemias attributable to enzyme disorders (D55.-)

Excludes 2 (Not Included Here)

  • Ehlers-Danlos syndromes (Q79.6-)
Instruction Source: E00-E89

Endocrine, nutritional and metabolic diseases

Excludes 1 (Mutually Exclusive)

  • transitory endocrine and metabolic disorders specific to newborn (P70-P74)

Clinical Notes

  • All neoplasms, whether functionally active or not, are classified in Chapter 2. Appropriate codes in this chapter (i.e. E05.8, E07.0, E16-E31, E34.-) may be used as additional codes to indicate either functional activity by neoplasms and ectopic endocrine tissue or hyperfunction and hypofunction of endocrine glands associated with neoplasms and other conditions classified elsewhere.
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