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Diagnosis Code

E80.3 DEFECTS OF CATALASE AND PEROXIDASE


Code Information

Diagnosis Code: E80.3

Short Description: Defects of catalase and peroxidase

Long Description: Defects of catalase and peroxidase

The code E80.3 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)
        • E80.3 Defects of catalase and peroxidase

Code Version: 2022 ICD-10-CM


Synonyms

  • Acatalasemia
  • Congenital hypothyroidism due to thyroid peroxidase mutation
  • Deficiency of catalase
  • Deficiency of cytochrome-c peroxidase
  • Deficiency of iodide peroxidase
  • Iodide peroxidase defect

References to Index of Diseases and Injuries

The code E80.3 has the following ICD-10-CM references to the Index of Diseases and Injuries
  • Inclusion Terms:
    • Acatalasia [Takahara]

Crosswalk Information

ICD-10 Code ICD-9 Code ICD-9 Description
E80.3 Right Arrow 277.89 Metabolism disorder NEC

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
E80.29 Other porphyria
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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