E80
Disorders of porphyrin and bilirubin metabolism
Header / non-billable
Choose the additional character
E80 needs more characters to be billable. Pick the specific code below.
- E80.0Hereditary erythropoietic porphyriaBillable
- E80.1Porphyria cutanea tardaBillable
- E80.2Other and unspecified porphyriaMore levels
- E80.3Defects of catalase and peroxidaseBillable
- E80.4Gilbert syndromeBillable
- E80.5Crigler-Najjar syndromeBillable
- E80.6Other disorders of bilirubin metabolismBillable
- E80.7Disorder of bilirubin metabolism, unspecifiedBillable
This code does not map to a risk-adjusting HCC in the loaded models.
Coding notes
Excludes 1 never coded together · Excludes 2 may co-exist
This code · E80
Includes
defects of catalase and peroxidase
Inherited from E70-E88Metabolic disorders
Inherited from chapter 4Endocrine, nutritional and metabolic diseases
Excludes 1
transitory endocrine and metabolic disorders specific to newborn (P70-P74)
Note
All neoplasms, whether functionally active or not, are classified in Chapter 2. Appropriate codes in this chapter (i.e. E05.8, E07.0, E16-E31, E34.-) may be used as additional codes to indicate either functional activity by neoplasms and ectopic endocrine tissue or hyperfunction and hypofunction of endocrine glands associated with neoplasms and other conditions classified elsewhere.