AutoICD API

E80.29

Billable

Other porphyria

Other porphyria

Status

Billable / Specific

Block

E70-E88

Parent Code

E80.2

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

Related Codes(2)
E80.20

Unspecified porphyria

BillableE80.21

Acute intermittent (hepatic) porphyria

Billable
Also Known As / Clinical Terms(155)

SNOMED CT

UMLS

Clinical Terms

  • Pink tooth
  • Uroporphyrinogen decarboxylase deficiency
  • Porphyrinuria
  • hereditary coproporphyria
  • Porphyria-like reaction
  • CPO - Coproporphyrinogen oxidase deficiency
  • Porphobilinogen synthase deficiency
  • Hematoporphyrinuria
  • PBGD deficiency
  • Congenital porphyria
  • Homozygous hereditary coproporphyria
  • Porphyrin within reference range
  • Harderoporphyria
  • Drug-induced porphyria
  • Coproporphyria
  • Skin lesion associated with hemodialysis
  • Ferrochelatase deficiency
  • hereditary coproporphyria porphyria
  • Pseudoporphyria due to PUVA therapy
  • Drug-induced pseudoporphyria
  • HO-1 (heme oxygenase-1) deficiency
  • Complication of hemodialysis
  • Uroporphyrinuria
  • Porphyria due to delta-aminolevulinate dehydratase deficiency
  • Adverse effect from psoralen and long-wave ultraviolet radiation photochemotherapy
  • Haematoporphyrinuria
  • PBGD - Porphobilinogen deaminase deficiency
  • Hemodialysis-associated pseudoporphyria
  • CPO deficiency
  • FECH - Ferrochelatase deficiency
  • Coproporphyrinogen Oxidase Deficiency
  • Complication of haemodialysis
  • Adverse effect from PUVA photochemotherapy
  • ALAD deficiency
  • Protoporphyrinuria
  • Hereditary delta-aminolevulinic aciduria
  • COPROPORPHYRIA, HEREDITARY
  • Pseudoporphyria
  • Haemodialysis-associated pseudoporphyria
  • Porphobilinogen deaminase deficiency
  • Coproporphyrinuria
  • Skin lesion associated with haemodialysis
  • CPOX DEFICIENCY
  • CPX DEFICIENCY
  • Uroporphyrinogen 1 synthase deficiency
  • ALA dehydratase deficiency porphyria
  • Pseudoporphyria in hemodialysis
  • HCP
  • Erythropoietic coproporphyria
  • HCP - Hereditary coproporphyria
  • Chester-type porphyria
  • Porphyruria
  • Inherited disorder of porphyrin metabolism
  • Porphyria of Doss
  • Porphyria hepatica II
  • Berger-Goldberg syndrome
  • Pseudoporphyria due to psoralen and long-wave ultraviolet radiation therapy
  • COPROPORPHYRINOGEN OXIDASE DEFIC
  • Delta-aminolaevulinate dehydrase deficiency
  • ALADH deficiency
  • Delta-aminolevulinate dehydrase deficiency
  • Hepatic porphyria
  • PUVA-induced pseudoporphyria
  • Hereditary coproporphyria (disorder)
  • CPRO deficiency
  • Uroporphyria
  • Deficiency, Coproporphyrinogen Oxidase
  • Heme oxygenase-1 deficiency
  • Pseudoporphyria in haemodialysis
  • Acute hepatic porphyria
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.

How does E80.29 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other porphyria 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 E80.29?

There is no direct ICD-11 mapping available for E80.29 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.

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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.