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Chapter IV

Disorders of porphyrin and bilirubin metabolism - E80


    Includes:
  • defects of catalase and peroxidase
E80.0 Hereditary erythropoietic porphyria
Congenital erythropoietic porphyria
Erythropoietic protoporphyria
E80.1 Porphyria cutanea tarda
E80.2 Other porphyria
Hereditary coproporphyria
Porphyria:
  • NOS
  • acute intermittent (hepatic)
    Use additional external cause code (Chapter XX), if desired, to identify cause.
  • E80.3 Defects of catalase and peroxidase
    Acatalasia [Takahara]
    E80.4 Gilbert's syndrome
    E80.5 Crigler-Najjar syndrome
    E80.6 Other disorders of bilirubin metabolism
    Dubin-Johnson syndrome
    Rotor's syndrome
    E80.7 Disorder of bilirubin metabolism, unspecified


    Related drugs:




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