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Diagnosis Code

E80.0 HEREDITARY ERYTHROPOIETIC PORPHYRIA


Code Information

Diagnosis Code: E80.0

Short Description: Hereditary erythropoietic porphyria

Long Description: Hereditary erythropoietic porphyria

The code E80.0 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)
        • E80.0 Hereditary erythropoietic porphyria

Code Version: 2022 ICD-10-CM


Synonyms

  • Congenital erythropoietic porphyria
  • Congenital porphyria
  • Congenital porphyria
  • Erythropoietic porphyria
  • Erythropoietic protoporphyria
  • Erythropoietic protoporphyria
  • Erythropoietic protoporphyria due to ferrochelatase deficiency
  • Erythropoietic protoporphyria due to gain of function of erythroid-specific aminolevulinic acid synthase 2
  • Erythropoietic uroporphyria associated with myeloid malignancy
  • Ferrochelatase deficiency
  • Ferrochelatase deficiency
  • Ferrochelatase deficiency
  • Ferrochelatase deficiency
  • Ferrochelatase deficiency
  • Homozygous erythropoietic protoporphyria
  • Porphyruria
  • Uroporphyrinuria
  • X-linked dominant erythropoietic protoporphyria

References to Index of Diseases and Injuries

The code E80.0 has the following ICD-10-CM references to the Index of Diseases and Injuries
  • Inclusion Terms:
    • Congenital erythropoietic porphyria
    • Erythropoietic protoporphyria

Crosswalk Information

ICD-10 Code ICD-9 Code ICD-9 Description
E80.0 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
E80.1 Porphyria cutanea tarda
E80.2 Other and unspecified porphyria
E80.20 Unspecified porphyria
E80.21 Acute intermittent (hepatic) porphyria
E80.29 Other 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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