Skip to content

E80.3

Billable

Defects of catalase and peroxidase

HCC Category Mapping

V28HCC 50Glycogen/Amino-Acid/Other Metabolic Disorders
0.289
V24HCC 23Other Significant Endocrine and Metabolic Disorders
0.230
ESRDHCC 23Other Significant Endocrine and Metabolic Disorders
0.000
RxHCCHCC 43Other Significant Endocrine and Metabolic Disorders
0.000

What This Code Means

A rare genetic condition where the body lacks or has defective enzymes (catalase or peroxidase) that normally break down harmful hydrogen peroxide in cells.

Coding Tips

  • This is a rare metabolic disorder; ensure documentation clearly identifies the specific enzyme deficiency
  • May be associated with other systemic manifestations that should be coded separately

Clinical Significance

Defects of catalase and peroxidase includes acatalasia (catalase deficiency), also known as Takahara disease. While often asymptomatic, affected individuals may develop oral ulcerations and gangrene due to inability to decompose hydrogen peroxide. Myeloperoxidase deficiency, the most common inherited neutrophil disorder, is also captured here.

Documentation Requirements

  • Specific enzyme deficiency documented (catalase deficiency/acatalasia or peroxidase deficiency/myeloperoxidase deficiency)
  • Confirmatory enzyme activity testing or genetic testing
  • Clinical manifestations: oral ulcers and gangrene (acatalasia), recurrent infections (myeloperoxidase deficiency)
  • Functional impact on patient's health
  • Treatment and management plan

Commonly Confused Codes

Code Hierarchy

Open E80.3 in the Interactive Encoder

See full code details, AI coding tips, HCC mappings, and related codes in our interactive encoder. Start your 14-day Pro trial — no credit card required.