 E80 |
 |
Disorders of porphyrin and bilirubin metabolism  |
| |
| Includes |
defects of catalase and peroxidase
|
|
| |
 E80.0 |
|
Hereditary erythropoietic porphyria |
| |
| Congenital erythropoietic porphyria | | Erythropoietic protoporphyria |
|
|
| |
| E80.1 |
|
Porphyria cutanea tarda |
|
| |
| E80.2 |
|
Other and unspecified porphyria |
| |
| E80.20 |
|
Unspecified porphyria |
| |
|
| | |
| E80.21 |
|
Acute intermittent (hepatic) porphyria |
| | |
| E80.29 |
|
Other porphyria |
| |
| Hereditary coproporphyria |
|
| |
| |
| E80.3 |
|
Defects of catalase and peroxidase |
| |
|
|
| |
| E80.4 |
|
Gilbert 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 |
|