E79.0
BillableHyperuricemia w/o signs of inflam arthrit and tophaceous dis
Hyperuricemia without signs of inflammatory arthritis and tophaceous disease
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Asymptomatic hyperuricemia
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(4)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(73)
SNOMED CT
- Hyperuricaemia35885006
- Hyperuricemia35885006
- Uricacidaemia35885006
- Uricacidemia35885006
- Increased uric acid level49099001
- Uric acid level above reference range49099001
- Blood urate abnormal166735007
- Blood urate outside reference range166735007
- Asymptomatic hyperuricemia190920002
- Hyperuricaemia without signs of inflammatory arthritis and tophaceous disease190920002
- Hyperuricemia without signs of inflammatory arthritis and tophaceous disease190920002
- Urate nephropathy236495001
- Uric acid nephropathy236495001
- Blood urate above reference range269859006
- Blood urate raised269859006
- Panniculitis due to crystal deposition402688004
- Panniculitis due to hyperuricaemia403419003
- Panniculitis due to hyperuricemia403419003
- Familial juvenile hyperuricaemic nephropathy type 2721840000
- Familial juvenile hyperuricemic nephropathy type 2721840000
- Hyperuricaemia, anaemia, renal failure syndrome721840000
- Hyperuricemia, anemia, renal failure syndrome721840000
- Renin associated familial juvenile hyperuricaemic nephropathy721840000
- Renin associated familial juvenile hyperuricemic nephropathy721840000
- Autosomal dominant medullary cystic kidney disease with hyperuricaemia723373006
- Autosomal dominant medullary cystic kidney disease with hyperuricemia723373006
- Medullary cystic kidney disease 2723373006
- UMOD-related autosomal dominant tubulointerstitial kidney disease723373006
- Uromodulin related autosomal dominant tubulointerstitial kidney disease723373006
- Autosomal dominant medullary cystic kidney disease726018006
- Autosomal dominant tubulointerstitial kidney disease726018006
- HUPRA syndrome776416004
- Hyperuricaemia, pulmonary hypertension, renal failure, alkalosis syndrome776416004
- Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome776416004
UMLS
- Asymptomatic hyperuricemiaC0281782
- Hyperuricaemia without signs of inflammatory arthritis and tophaceous diseaseC0348944
- Hyperuricemia w/o signs of inflam arthrit and tophaceous disC0348944
- Hyperuricemia without signs of inflammatory arthritis and tophaceous diseaseC0348944
- Hyperuricemia without signs of inflammatory arthritis and tophaceous disease (disorder)C0348944
Clinical Terms
- Panniculitis due to hyperuricemia
- Hyperuricaemia
- Hyperuricemia without signs of inflammatory arthritis and tophaceous disease (disorder)
- Uric acid level above reference range
- Increased uric acid level
- Blood urate abnormal
- Autosomal dominant medullary cystic kidney disease with hyperuricaemia
- Blood urate raised
- Autosomal dominant tubulointerstitial kidney disease
- Blood urate outside reference range
- Familial juvenile hyperuricemic nephropathy type 2
- Autosomal dominant medullary cystic kidney disease with hyperuricemia
- Hyperuricaemia without signs of inflammatory arthritis and tophaceous disease
- Panniculitis due to hyperuricaemia
- UMOD-related autosomal dominant tubulointerstitial kidney disease
- Autosomal dominant medullary cystic kidney disease
- Renin associated familial juvenile hyperuricemic nephropathy
- Familial juvenile hyperuricaemic nephropathy type 2
- Hyperuricemia, anemia, renal failure syndrome
- Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome
- Hyperuricemia
- Uricacidemia
- HUPRA syndrome
- Uric acid nephropathy
- Hyperuricaemia, anaemia, renal failure syndrome
- Asymptomatic hyperuricemia
- Uricacidaemia
- Medullary cystic kidney disease 2
- Blood urate above reference range
- Hyperuricaemia, pulmonary hypertension, renal failure, alkalosis syndrome
- Urate nephropathy
- Panniculitis due to crystal deposition
- Renin associated familial juvenile hyperuricaemic nephropathy
- Uromodulin related autosomal dominant tubulointerstitial kidney disease
Frequently Asked Questions
What is the ICD-10 code for hyperuricemia w/o signs of inflam arthrit and tophaceous dis?
The ICD-10-CM code for hyperuricemia w/o signs of inflam arthrit and tophaceous dis is E79.0. The full clinical description is "Hyperuricemia without signs of inflammatory arthritis and tophaceous disease". E79.0 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E79.0 mean?
ICD-10-CM code E79.0 represents “Hyperuricemia without signs of inflammatory arthritis and tophaceous disease”. 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 E79.0 a billable code?
Yes, E79.0 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E79.0 in?
E79.0 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E79.0?
E79.0 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 E79.0 map to?
E79.0 maps to 12 SNOMED CT concepts: 190920002, 726018006, 723373006, 166735007, 269859006, and 7 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E79.0?
E79.0 is linked to 2 UMLS Concept Unique Identifiers: C0281782, C0348944. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E79.0 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like hyperuricemia w/o signs of inflam arthrit and tophaceous dis 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 E79.0?
E79.0 maps to the ICD-11 code: 5C55.Y (Other specified inborn errors of purine, pyrimidine or nucleotide metabolism).
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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.