E80.29
BillableOther porphyria
Other porphyria
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Hereditary coproporphyria
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
- Berger-Goldberg syndrome7425008
- CPO - Coproporphyrinogen oxidase deficiency7425008
- CPO deficiency7425008
- CPRO deficiency7425008
- Coproporphyrinogen oxidase deficiency7425008
- HCP - Hereditary coproporphyria7425008
- Hereditary coproporphyria7425008
- Porphyria hepatica II7425008
- Drug-induced porphyria43599001
- Haematoporphyrinuria44574006
- Hematoporphyrinuria44574006
- Pink tooth44574006
- Porphyrinuria44574006
- Porphyruria44574006
- Hepatic porphyria55056006
- Erythropoietic coproporphyria61164006
- ALA dehydratase deficiency porphyria64081000
- ALAD deficiency64081000
- ALADH deficiency64081000
- Acute hepatic porphyria64081000
- Delta-aminolaevulinate dehydrase deficiency64081000
- Delta-aminolevulinate dehydrase deficiency64081000
- Hereditary delta-aminolevulinic aciduria64081000
- Porphobilinogen synthase deficiency64081000
- Porphyria due to delta-aminolevulinate dehydratase deficiency64081000
- Porphyria of Doss64081000
- Chester-type porphyria84816006
- Complication of haemodialysis85223007
- Complication of hemodialysis85223007
- Pseudoporphyria95565000
- Uroporphyria123964001
- Uroporphyrinuria123964001
- Coproporphyrinuria123965000
- Protoporphyrinuria123966004
- Congenital porphyria190913009
- Coproporphyria190915002
- Harderoporphyria238056003
- Homozygous hereditary coproporphyria238056003
- Drug-induced pseudoporphyria239000007
- Porphyria-like reaction239000007
- Uroporphyrinogen decarboxylase deficiency276262000
- PBGD - Porphobilinogen deaminase deficiency276263005
- PBGD deficiency276263005
- Porphobilinogen deaminase deficiency276263005
- Uroporphyrinogen 1 synthase deficiency276263005
- FECH - Ferrochelatase deficiency276265003
- Ferrochelatase deficiency276265003
- Skin lesion associated with haemodialysis402762007
- Skin lesion associated with hemodialysis402762007
- Adverse effect from PUVA photochemotherapy403710000
- Adverse effect from psoralen and long-wave ultraviolet radiation photochemotherapy403710000
- PUVA-induced pseudoporphyria403717002
- Pseudoporphyria due to PUVA therapy403717002
- Pseudoporphyria due to psoralen and long-wave ultraviolet radiation therapy403717002
- Haemodialysis-associated pseudoporphyria403732009
- Hemodialysis-associated pseudoporphyria403732009
- Pseudoporphyria in haemodialysis403732009
- Pseudoporphyria in hemodialysis403732009
- Inherited disorder of porphyrin metabolism403832004
- Porphyrin within reference range1186598009
- HO-1 (heme oxygenase-1) deficiency1230003009
- Heme oxygenase-1 deficiency1230003009
UMLS
- Berger-Goldberg syndromeC0162531
- COPROPORPHYRIA, HEREDITARYC0162531
- COPROPORPHYRINOGEN OXIDASE DEFICC0162531
- COPROPORPHYRINOGEN OXIDASE DEFICIENCYC0162531
- CPO - Coproporphyrinogen oxidase deficiencyC0162531
- CPO DEFICIENCYC0162531
- CPO deficiencyC0162531
- CPOX DEFICIENCYC0162531
- CPRO deficiencyC0162531
- CPX DEFICIENCYC0162531
- Coproporphyria, HereditaryC0162531
- Coproporphyrinogen Oxidase DeficiencyC0162531
- Coproporphyrinogen oxidase deficiencyC0162531
- Deficiency, Coproporphyrinogen OxidaseC0162531
- HCPC0162531
- HCP - Hereditary coproporphyriaC0162531
- Hereditary CoproporphyriaC0162531
- Hereditary coproporphyriaC0162531
- Hereditary coproporphyria (disorder)C0162531
- Porphyria hepatica IIC0162531
- hereditary coproporphyriaC0162531
- hereditary coproporphyria porphyriaC0162531
- Other porphyriaC0348496
Frequently Asked Questions
What is the ICD-10 code for other porphyria?
The ICD-10-CM code for other porphyria is E80.29. The full clinical description is "Other porphyria". E80.29 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E80.29 mean?
ICD-10-CM code E80.29 represents "Other porphyria". It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a billable/specific code that can be used on a claim.
Is E80.29 a billable code?
Yes, E80.29 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E80.29 in?
E80.29 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E80.29?
E80.29 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 E80.29 map to?
E80.29 maps to 26 SNOMED CT concepts: 64081000, 403710000, 7425008, 84816006, 85223007, and 21 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E80.29?
E80.29 is linked to 2 UMLS Concept Unique Identifiers: C0162531, C0348496. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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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.