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Diagnosis Code

E80.29 OTHER PORPHYRIA


Code Information

Diagnosis Code: E80.29

Short Description: Other porphyria

Long Description: Other porphyria

The code E80.29 is VALID for claim submission

Code Classification:

  • Endocrine, nutritional and metabolic diseases (E00–E89)
    • Metabolic disorders (E70-E88)
      • Disorders of porphyrin and bilirubin metabolism (E80)
        • E80.29 Other porphyria

Code Version: 2022 ICD-10-CM


Synonyms

  • Adverse effect from PUVA photochemotherapy
  • Chester-type porphyria
  • Complication of hemodialysis
  • Congenital porphyria
  • Coproporphyria
  • Coproporphyrinuria
  • Drug-induced porphyria
  • Drug-induced pseudoporphyria
  • Erythropoietic coproporphyria
  • Ferrochelatase deficiency
  • Heme oxygenase-1 deficiency
  • Hemodialysis-associated pseudoporphyria
  • Hepatic porphyria
  • Hereditary coproporphyria
  • Homozygous hereditary coproporphyria
  • Inherited disorder of porphyrin metabolism
  • Porphobilinogen deaminase deficiency
  • Porphobilinogen synthase deficiency
  • Porphyruria
  • Porphyruria
  • Protoporphyrinuria
  • Pseudoporphyria
  • Pseudoporphyria
  • Pseudoporphyria
  • Pseudoporphyria
  • Pseudoporphyria due to PUVA therapy
  • Skin lesion associated with hemodialysis
  • Uroporphyrinogen decarboxylase deficiency
  • Uroporphyrinuria

References to Index of Diseases and Injuries

The code E80.29 has the following ICD-10-CM references to the Index of Diseases and Injuries
  • Inclusion Terms:
    • Hereditary coproporphyria

Crosswalk Information

ICD-10 Code ICD-9 Code ICD-9 Description
E80.29 Right Arrow 277.1 Dis porphyrin metabolism

This ICD-10 to ICD-9 data is based on the 2018 General Equivalency Mapping (GEM) files published by the Centers for Medicare & Medicaid Services (CMS) for informational purposes only. The data is not an ICD-10 conversion tool and doesn’t guarantee clinical accuracy.

Similar Codes

ICD-10 Code ICD-10 Description
E80 Disorders of porphyrin and bilirubin metabolism
E80.0 Hereditary erythropoietic porphyria
E80.1 Porphyria cutanea tarda
E80.2 Other and unspecified porphyria
E80.20 Unspecified porphyria
E80.21 Acute intermittent (hepatic) porphyria
E80.3 Defects of catalase and peroxidase
E80.4 Gilbert syndrome
E80.5 Crigler-Najjar syndrome
E80.6 Other disorders of bilirubin metabolism
E80.7 Disorder of bilirubin metabolism, unspecified

This page was last updated on: 10/1/2023

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