kodex

Kodex

E74.00

Glycogen storage disease, unspecified

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Hierarchy

  • E00-E89 Endocrine, nutritional and metabolic diseases (E00-E89)
    • E70-E88 Metabolic disorders (E70-E88)
      • E74 Other disorders of carbohydrate metabolism
        • E74.0 Glycogen storage disease
          • E74.00 Glycogen storage disease, unspecified
          • E74.01 von Gierke disease
          • E74.02 Pompe disease
          • E74.03 Cori disease
          • E74.04 McArdle disease
          • E74.05 Lysosome-associated membrane protein 2 [LAMP2] deficiency
          • E74.09 Other glycogen storage disease

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

Excludes 1

E74

  • E08-E13 Diabetes mellitus (E08-E13)
  • hypoglycemia NOS (E16.2)
    • E16.2 Hypoglycemia, unspecified
  • E16.3 Increased secretion of glucagon
  • mucopolysaccharidosis (E76.0-E76.3)

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

E70-E88

  • Q79.6 Ehlers-Danlos syndromes