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:

E80.3 - Defects of catalase and peroxidase:

• Citric Acid; Potassium Bicarbonate; Sodium Citrate

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The information was verified by Dr. Rachana Salvi, MD Pharmacology

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