kodex

Kodex

E75.4

Neuronal ceroid lipofuscinosis

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Hierarchy

  • E00-E89 Endocrine, nutritional and metabolic diseases (E00-E89)
    • E70-E88 Metabolic disorders (E70-E88)
      • E75 Disorders of sphingolipid metabolism and other lipid storage disorders
        • E75.0 GM2 gangliosidosis
        • E75.1 Other and unspecified gangliosidosis
        • E75.2 Other sphingolipidosis
        • E75.3 Sphingolipidosis, unspecified
        • E75.4 Neuronal ceroid lipofuscinosis
        • E75.5 Other lipid storage disorders
        • E75.6 Lipid storage disorder, unspecified

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

E75.4

  • Batten disease
  • Bielschowsky-Jansky disease
  • Kufs disease
  • Spielmeyer-Vogt disease

Excludes 1

E75

  • mucolipidosis, types I-III (E77.0-E77.1)
  • G60.1 Refsum's disease

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