E80.3
BillableDefects of catalase and peroxidase
Defects of catalase and peroxidase
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Acatalasia [Takahara]
Includes
Conditions included under this code
- defects of catalase and peroxidase
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Related Codes(7)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(28)
SNOMED CT
- Defective iodide peroxidase activity81873006
- Iodide peroxidase defect81873006
- Deficiency of cytochrome-c peroxidase124201006
- Deficiency of catalase124202004
- Deficiency of iodide peroxidase124204003
- Deficiency of iodinase124204003
- Acatalasaemia267454002
- Acatalasemia267454002
- Acatalasia267454002
- Catalase deficiency267454002
- Takahara disease267454002
- Congenital hypothyroidism due to thyroid peroxidase mutation1179394003
UMLS
Clinical Terms
- Catalase deficiency
- Defective iodide peroxidase activity
- Deficiency of iodide peroxidase
- Deficiency of catalase
- Acatalasaemia
- Deficiency of cytochrome-c peroxidase
- Deficiency of iodinase
- Iodide peroxidase defect
- Takahara disease
- Congenital hypothyroidism due to thyroid peroxidase mutation
- Acatalasia
- Acatalasemia
- Acatalasia [Takahara]
Frequently Asked Questions
What is the ICD-10 code for defects of catalase and peroxidase?
The ICD-10-CM code for defects of catalase and peroxidase is E80.3. The full clinical description is "Defects of catalase and peroxidase". E80.3 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E80.3 mean?
ICD-10-CM code E80.3 represents “Defects of catalase and peroxidase”. 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 E80.3 a billable code?
Yes, E80.3 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E80.3 in?
E80.3 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E80.3?
E80.3 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 E80.3 map to?
E80.3 maps to 6 SNOMED CT concepts: 267454002, 1179394003, 81873006, 124202004, 124201006, and 1 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E80.3?
E80.3 is linked to 2 UMLS Concept Unique Identifiers: C2874296, C0494349. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E80.3 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like defects of catalase and peroxidase 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 E80.3?
E80.3 maps to the ICD-11 code: 5C58.Z (Inborn errors of porphyrin or heme metabolism, unspecified).
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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.