kodex

Kodex

E71.313

Glutaric aciduria type II

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Hierarchy

  • E00-E89 Endocrine, nutritional and metabolic diseases (E00-E89)
    • E70-E88 Metabolic disorders (E70-E88)
      • E71 Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
        • E71.3 Disorders of fatty-acid metabolism
          • 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

Notes

E00-E89

  • 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.
    • E07.0 Hypersecretion of calcitonin
    • E34 Other endocrine disorders

Inclusion Terms

E71.313

  • Glutaric aciduria type II A
  • Glutaric aciduria type II B
  • Glutaric aciduria type II C

Excludes 1

E71.313

  • glutaric aciduria (type 1) NOS (E72.3)
    • E72.3 Disorders of lysine and hydroxylysine metabolism

E71.3

  • E71.5 Peroxisomal disorders
  • G60.1 Refsum's disease
  • Schilder's disease (G37.0)
    • G37.0 Diffuse sclerosis of central nervous system

E70-E88

  • E34.5 Androgen insensitivity syndrome
  • congenital adrenal hyperplasia (E25.0)
    • E25.0 Congenital adrenogenital disorders associated with enzyme deficiency
  • hemolytic anemias attributable to enzyme disorders (D55.-)
    • D55 Anemia due to enzyme disorders
  • Q87.4 Marfan syndrome
  • 5-alpha-reductase deficiency (E29.1)
    • E29.1 Testicular hypofunction

E00-E89

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

Excludes 2

E71.3

  • carnitine deficiency due to inborn error of metabolism (E71.42)
    • E71.42 Carnitine deficiency due to inborn errors of metabolism

E70-E88

  • Q79.6 Ehlers-Danlos syndromes