| 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
|