kodex

Kodex

E88.02

Plasminogen deficiency

Copy Code Send Code

Hierarchy

  • E00-E89 Endocrine, nutritional and metabolic diseases (E00-E89)
    • E70-E88 Metabolic disorders (E70-E88)
      • E88 Other and unspecified metabolic disorders
        • E88.0 Disorders of plasma-protein metabolism, not elsewhere classified
          • E88.01 Alpha-1-antitrypsin deficiency
          • E88.02 Plasminogen deficiency
          • E88.09 Other disorders of plasma-protein metabolism, not elsewhere classified

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

E88.02

  • Dysplasminogenemia
  • Hypoplasminogenemia
  • Type 1 plasminogen deficiency
  • Type 2 plasminogen deficiency

Code Also

E88.02

  • , if applicable, ligneous conjunctivitis (H10.51)
    • H10.51 Ligneous conjunctivitis

Use Additional

E88.02

  • code for associated findings, such as:
  • hydrocephalus (G91.4)
    • G91.4 Hydrocephalus in diseases classified elsewhere
  • otitis media (H67.-)
    • H67 Otitis media in diseases classified elsewhere
  • respiratory disorder related to plasminogen deficiency (J99)
    • J99 Respiratory disorders in diseases classified elsewhere

E88

  • codes for associated conditions

Excludes 1

E88.0

  • D47.2 Monoclonal gammopathy
  • D89.0 Polyclonal hypergammaglobulinemia
  • Waldenström macroglobulinemia (C88.00)
    • C88.00 Waldenström macroglobulinemia not having achieved remission

E88

  • histiocytosis X (chronic) (C96.6)
    • C96.6 Unifocal Langerhans-cell histiocytosis

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

E88.0

  • disorder of lipoprotein metabolism (E78.-)
    • E78 Disorders of lipoprotein metabolism and other lipidemias

E70-E88

  • Q79.6 Ehlers-Danlos syndromes