E80.0
BillableHereditary erythropoietic porphyria
Hereditary erythropoietic porphyria
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Congenital erythropoietic porphyria
- Erythropoietic protoporphyria
Includes
Conditions included under this code
- defects of catalase and peroxidase
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
SNOMED CT
- CEP - Congenital erythropoietic porphyria22935002
- Congenital erythropoietic porphyria22935002
- Congenital photosensitive porphyria22935002
- Gunther's disease22935002
- Haematoporphyria congenita22935002
- Hematoporphyria congenita22935002
- Porphyria erythropoietica22935002
- Uroporphyrinogen III synthase deficiency22935002
- Haematoporphyrinuria44574006
- Hematoporphyrinuria44574006
- Pink tooth44574006
- Porphyrinuria44574006
- Porphyruria44574006
- EPP - erythropoietic protoporphyria51022005
- Erythrohepatic protoporphyria51022005
- Erythropoietic protoporphyria51022005
- Haem synthase deficiency51022005
- Heme synthase deficiency51022005
- Magnus syndrome51022005
- Protoporphyria51022005
- Erythropoietic porphyria67312003
- Uroporphyria123964001
- Uroporphyrinuria123964001
- Congenital porphyria190913009
- Homozygous erythropoietic protoporphyria238053006
- FECH - Ferrochelatase deficiency276265003
- Ferrochelatase deficiency276265003
- Erythropoietic uroporphyria associated with myeloid malignancy783615009
- Erythropoietic protoporphyria due to ferrochelatase deficiency860859009
- Erythropoietic protoporphyria due to gain of function of erythroid-specific aminolevulinic acid synthase 21186810009
- X-linked dominant erythropoietic protoporphyria1197360001
UMLS
- CEPC5886774
- CEP - Congenital erythropoietic porphyriaC5886774
- CONGEN ERYTHROPOIETIC PORPHYRIAC5886774
- Congenital Erythropoietic PorphyriaC5886774
- Congenital Erythropoietic PorphyriasC5886774
- Congenital erythropoietic porphyriaC5886774
- Congenital erythropoietic porphyria (disorder)C5886774
- Congenital photosensitive porphyriaC5886774
- Congenital porphyriaC5886774
- Congenital porphyria (disorder)C5886774
- Erythropoietic PorphyriaC5886774
- Erythropoietic Porphyria, CongenitalC5886774
- Erythropoietic PorphyriasC5886774
- Erythropoietic Porphyrias, CongenitalC5886774
- GUNTHER DISC5886774
- GUNTHER DISEASEC5886774
- GUNTHERS DISC5886774
- Gunther DiseaseC5886774
- Gunther's DiseaseC5886774
- Gunther's diseaseC5886774
- Gunthers DiseaseC5886774
- Haematoporphyria congenitaC5886774
- Hematoporphyria congenitaC5886774
- Hereditary erythropoietic porphyriaC5886774
- PORPHYRIA ERYTHROPOIETIC CONGENC5886774
- PORPHYRIA, CONGENITAL ERYTHROPOIETICC5886774
- Porphyria erythropoieticaC5886774
- Porphyria, Congenital ErythropoieticC5886774
- Porphyria, ErythropoieticC5886774
- Porphyria, Erythropoietic, CongenitalC5886774
- Porphyrias, Congenital ErythropoieticC5886774
- Porphyrias, ErythropoieticC5886774
- congenital erythropoietic porphyriaC5886774
- congenital photosensitive porphyriaC5886774
- congenital porphyriaC5886774
- erythropoietic porphyriaC5886774
- erythropoietic uroporphyriaC5886774
- gunther diseaseC5886774
- gunther's diseaseC5886774
- gunthers diseaseC5886774
- EPPC0162568
- EPP (erythropoietic protoporphyria porphyria)C0162568
- EPP - erythropoietic protoporphyriaC0162568
- ERYTHROHEPATIC PROTOPORPHYRIAC0162568
- Erythrohepatic ProtoporphyriaC0162568
- Erythrohepatic protoporphyriaC0162568
- Erythropoietic ProtoporphyriaC0162568
- Erythropoietic ProtoporphyriasC0162568
- Erythropoietic protoporphyriaC0162568
- Erythropoietic protoporphyria (disorder)C0162568
- Magnus syndromeC0162568
- PROTOPORPHYRIA, ERYTHROPOIETICC0162568
- ProtoporphyriaC0162568
- Protoporphyria, ErythropoieticC0162568
- Protoporphyrias, ErythropoieticC0162568
- eppC0162568
- erythrohepatic protoporphyriaC0162568
- erythropoietic protoporphyriaC0162568
- magnus syndromeC0162568
- protoporphyriaC0162568
- protoporphyria erythropoieticC0162568
Frequently Asked Questions
What is ICD-10 code E80.0?
ICD-10-CM code E80.0 represents "Hereditary erythropoietic porphyria". It is a billable/specific code that can be used on a claim.
Is E80.0 a billable code?
Yes, E80.0 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E80.0 in?
E80.0 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E80.0?
E80.0 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 SNOMED CT codes does E80.0 map to?
E80.0 maps to 12 SNOMED CT concepts: 22935002, 190913009, 51022005, 67312003, 860859009, and 7 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E80.0?
E80.0 is linked to 2 UMLS Concept Unique Identifiers: C5886774, C0162568. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
Automate ICD-10 Coding With AI
Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.
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.