E80
Non-billableDisorders of porphyrin and bilirubin metabolism
Disorders of porphyrin and bilirubin metabolism
This is a header/category code. For billing purposes, use a more specific child code from the list below.
Coding Notes
Includes
Conditions included under this code
- defects of catalase and peroxidase
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Child Codes (8)
E80.0Hereditary erythropoietic porphyria
E80.1Porphyria cutanea tarda
E80.2Other and unspecified porphyria
E80.3Defects of catalase and peroxidase
E80.4Gilbert syndrome
E80.5Crigler-Najjar syndrome
E80.6Other disorders of bilirubin metabolism
E80.7Disorder of bilirubin metabolism, unspecified
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(3)
Frequently Asked Questions
What is the ICD-10 code for disorders of porphyrin and bilirubin metabolism?
The ICD-10-CM code for disorders of porphyrin and bilirubin metabolism is E80. The full clinical description is "Disorders of porphyrin and bilirubin metabolism". E80 is a non-billable header code. Use a more specific child code for billing purposes.
What does ICD-10 code E80 mean?
ICD-10-CM code E80 represents “Disorders of porphyrin and bilirubin metabolism”. It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a non-billable header code. Use a more specific child code for billing purposes.
Is E80 a billable code?
No, E80 is a non-billable header code. You need to use one of its more specific child codes for billing. There are 8 child codes under E80.
What chapter is E80 in?
E80 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E80?
E80 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); and 3 more.
What are the subcategories under E80?
E80 has 8 child codes, including: E80.0 (Hereditary erythropoietic porphyria), E80.1 (Porphyria cutanea tarda), E80.2 (Other and unspecified porphyria), E80.3 (Defects of catalase and peroxidase), and 4 more.
What are the UMLS CUIs for E80?
E80 is linked to 2 UMLS Concept Unique Identifiers: C0494349, C0494347. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E80 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like disorders of porphyrin and bilirubin metabolism affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of E80?
E80 maps to the ICD-11 code: 5C58.Z (Inborn errors of porphyrin or heme metabolism, unspecified).
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.