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 newborn (P70-P74)
- androgen insensitivity syndrome (E34.5-)
- congenital adrenal hyperplasia (E25.0)
- hemolytic anemias attributable to enzyme disorders (D55.-)
- Marfan syndrome (Q87.4-)
- 5-alpha-reductase deficiency (E29.1)
- Ataxia-telangiectasia (Q87.19)
- Bloom's syndrome (Q82.8)
- Cockayne's syndrome (Q87.19)
- calculus of kidney (N20.0)
- combined immunodeficiency disorders (D81.-)
- Fanconi's anemia (D61.09)
- gout (M1A.-, M10.-)
- orotaciduric anemia (D53.0)
- progeria (E34.8)
- Werner's syndrome (E34.8)
- xeroderma pigmentosum (Q82.1)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
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
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.
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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.