Kodex

Code

E83.110

Hereditary hemochromatosis

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Hierarchy

E00-E89 Endocrine, nutritional and metabolic diseases (E00-E89)
- E70-E88 Metabolic disorders (E70-E88)
  - E83 Disorders of mineral metabolism
    - E83.1 Disorders of iron metabolism
      - E83.11 Hemochromatosis
        
        E83.110 Hereditary hemochromatosis
        
        E83.111 Hemochromatosis due to repeated red blood cell transfusions
        
        E83.118 Other hemochromatosis
        
        E83.119 Hemochromatosis, unspecified

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

Inclusion Terms

E83.110

Bronzed diabetes
Pigmentary cirrhosis (of liver)
Primary (hereditary) hemochromatosis

Excludes 1

GALD (P78.84)
- P78.84 Gestational alloimmune liver disease
P78.84 Gestational alloimmune liver disease
Neonatal hemochromatosis (P78.84)
- P78.84 Gestational alloimmune liver disease

D50 Iron deficiency anemia
sideroblastic anemia (D64.0-D64.3)

dietary mineral deficiency (E58-E61)
parathyroid disorders (E20-E21)
E55 Vitamin D deficiency

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's syndrome
5-alpha-reductase deficiency (E29.1)
- E29.1 Testicular hypofunction

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

Excludes 2

Q79.6 Ehlers-Danlos syndromes