Code
Hierarchy
-
E00-E89 Endocrine, nutritional and metabolic diseases (E00-E89)
-
E70-E88 Metabolic disorders (E70-E88)
-
E80 Disorders of porphyrin and bilirubin metabolism
-
E80.0 Hereditary erythropoietic porphyria
-
E80.1 Porphyria cutanea tarda
-
E80.2 Other and unspecified porphyria
-
E80.3 Defects of catalase and peroxidase
-
E80.4 Gilbert syndrome
-
E80.5 Crigler-Najjar syndrome
-
E80.6 Other disorders of bilirubin metabolism
-
E80.7 Disorder of bilirubin metabolism, 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.
Includes
-
defects of catalase and peroxidase
Excludes 1
- 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
- P70-P74 Transitory endocrine and metabolic disorders specific to newborn (P70-P74)