E79.82
BillableHereditary xanthinuria
Hereditary xanthinuria
Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- •transitory endocrine and metabolic disorders specific to newbornP70-P74
- •androgen insensitivity syndromeE34.5
- •congenital adrenal hyperplasiaE25.0
- •hemolytic anemias attributable to enzyme disordersD55
- •Marfan syndromeQ87.4
- •5-alpha-reductase deficiencyE29.1
- •Ataxia-telangiectasiaQ87.19
- •Bloom's syndromeQ82.8
- •Cockayne's syndromeQ87.19
- •calculus of kidneyN20.0
- •combined immunodeficiency disordersD81
- •Fanconi's anemiaD61.09
- •gout (M1A.-,M10
- •orotaciduric anemiaD53.0
- •progeriaE34.8
- •Werner's syndromeE34.8
- •xeroderma pigmentosumQ82.1
Related Codes(2)
Also Known As / Clinical Terms(45)
SNOMED CT
- Combined molybdoflavoprotein enzyme deficiency29692004
- Combined xanthine oxidase and aldehyde oxidase deficiency29692004
- Combined xanthine oxidase and sulfite oxidase and aldehyde oxidase deficiency29692004
- Combined xanthine oxidase and sulphite oxidase and aldehyde oxidase deficiency29692004
- Deficiency of molybdenum cofactor29692004
- Hereditary xanthinuria type 229692004
- Hereditary xanthinuria, type 229692004
- Molybdenum cofactor deficiency29692004
- Xanthine oxidase-sulfite oxidase deficiency29692004
- Xanthine oxidase-sulphite oxidase deficiency29692004
- Classical xanthinuria54627004
- Hereditary xanthinuria54627004
- Deficiency of hypoxanthine oxidase124147007
- Deficiency of xanthine oxidase124147007
- Xanthine oxidase deficiency124147007
- Xanthinuria190919008
- Hereditary xanthinuria type 1836343001
- Xanthinuria type I836343001
- Molybdenum cofactor deficiency complementation group A1003367004
- Molybdenum cofactor deficiency complementation group B1003368009
- Molybdenum cofactor deficiency complementation group C1003387003
UMLS
Clinical Terms
- Xanthine oxidase-sulphite oxidase deficiency
- Deficiency of hypoxanthine oxidase
- Hereditary xanthinuria, type 2
- Hereditary xanthinuria type 2
- Deficiency of xanthine oxidase
- Classical xanthinuria
- Xanthinuria
- Combined xanthine oxidase and sulphite oxidase and aldehyde oxidase deficiency
- Combined molybdoflavoprotein enzyme deficiency
- Xanthine oxidase deficiency
- Hereditary xanthinuria (disorder)
- Deficiency of molybdenum cofactor
- Hereditary xanthinuria type 1
- Molybdenum cofactor deficiency complementation group C
- Combined xanthine oxidase and aldehyde oxidase deficiency
- Xanthinuria type I
- Molybdenum cofactor deficiency complementation group A
- Molybdenum cofactor deficiency complementation group B
- Molybdenum cofactor deficiency
- Combined xanthine oxidase and sulfite oxidase and aldehyde oxidase deficiency
- Xanthine oxidase-sulfite oxidase deficiency
Frequently Asked Questions
What is the ICD-10 code for hereditary xanthinuria?
The ICD-10-CM code for hereditary xanthinuria is E79.82. The full clinical description is "Hereditary xanthinuria". E79.82 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E79.82 mean?
ICD-10-CM code E79.82 represents “Hereditary xanthinuria”. 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 E79.82 a billable code?
Yes, E79.82 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E79.82 in?
E79.82 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E79.82?
E79.82 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 14 more.
What SNOMED CT codes does E79.82 map to?
E79.82 maps to 8 SNOMED CT concepts: 54627004, 29692004, 124147007, 836343001, 1003367004, and 3 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E79.82?
E79.82 is linked to 1 UMLS Concept Unique Identifier: C5779508. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E79.82 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like hereditary xanthinuria 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 E79.82?
There is no direct ICD-11 mapping available for E79.82 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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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.