E80 – Disorders of porphyrin and bilirubin metabolism
Coding Notes
Active
Non-billable / Non-specific, not valid for HIPAA-covered transactions
Includes
defects of catalase and peroxidase
Child Codes
Sibling Codes
View in Tabular
| Code | Title |
|---|---|
| E00-E89 | Endocrine, nutritional and metabolic diseases (E00-E89) |
| E70-E88 | Metabolic disorders (E70-E88) |
| E80 |
Disorders of porphyrin and bilirubin metabolism
Includes
defects of catalase and peroxidase
|
| E80.0 | Hereditary erythropoietic porphyria |
| 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 |
| 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 |