E79.1
BillableLesch-Nyhan syndrome
Lesch-Nyhan syndrome
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- HGPRT deficiency
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
- Choreoathetosis self-mutilation syndrome10406007
- Complete HGPRT deficiency10406007
- Complete hypoxanthine-guanine phosphoribosyltransferase deficiency10406007
- HGPRT deficiency10406007
- HPRT - Hypoxanthine-guanine phosphoribosyltransferase deficiency10406007
- Hypoxanthine-guanine phosphoribosyltransferase deficiency10406007
- Lesch-Nyhan disease10406007
- Lesch-Nyhan syndrome10406007
- Total HGPRT deficiency10406007
- X-linked hyperuricaemia10406007
- X-linked hyperuricemia10406007
- Hyperuricaemia35885006
- Hyperuricemia35885006
- Uricacidaemia35885006
- Uricacidemia35885006
- Deficiency of IMP pyrophosphorylase124275001
- Deficiency of guanine phosphoribosyltransferase124275001
- Deficiency of hypoxanthine phosphoribosyltransferase124275001
- Deficiency of hypoxanthine-guanine phosphoribosyltransferase124275001
- Blood urate abnormal166735007
- Blood urate outside reference range166735007
- Partial HGPRT deficiency238007004
- Partial hypoxanthine-guanine phosphoribosyltransferase deficiency238007004
- Blood urate above reference range269859006
- Blood urate raised269859006
- Chorea due to metabolic disorder1259619002
- Chorea due to Lesch-Nyhan syndrome1259654009
- Dystonia due to Lesch Nyhan syndrome1260390003
UMLS
- COMPLETE HGPRT DEFIC DISC0023374
- Choreoathetosis Self Mutilation Hyperuricemia SyndromeC0023374
- Choreoathetosis Self Mutilation SyndromeC0023374
- Choreoathetosis Self-Mutilation Hyperuricemia SyndromeC0023374
- Choreoathetosis Self-Mutilation SyndromeC0023374
- Choreoathetosis Self-Mutilation SyndromesC0023374
- Choreoathetosis self-mutilation syndromeC0023374
- Complete HGPRT Deficiency DiseaseC0023374
- Complete HGPRT deficiencyC0023374
- Complete HPRT DeficienciesC0023374
- Complete HPRT DeficiencyC0023374
- Complete HPRT deficiencyC0023374
- Complete Hypoxanthine Guanine Phosphoribosyltransferase DeficiencyC0023374
- Complete Hypoxanthine-Guanine Phosphoribosyltransferase DeficiencyC0023374
- Complete hypoxanthine-guanine phosphoribosyltransferase deficiencyC0023374
- DEFIC DIS COMPLETE HGPRTC0023374
- DEFIC DIS HYPOXANTHINE PHOSPHORIBOSYL TRANSFERASEC0023374
- Deficiencies, Complete HPRTC0023374
- Deficiencies, HGPRTC0023374
- Deficiencies, Hypoxanthine PhosphoribosyltransferaseC0023374
- Deficiencies, Total HPRTC0023374
- Deficiency Disease, Complete HGPRTC0023374
- Deficiency Disease, Hypoxanthine Phosphoribosyl TransferaseC0023374
- Deficiency Disease, Hypoxanthine-Phosphoribosyl-TransferaseC0023374
- Deficiency Diseases, Hypoxanthine-Phosphoribosyl-TransferaseC0023374
- Deficiency of Guanine PhosphoribosyltransferaseC0023374
- Deficiency of Hypoxanthine PhosphoribosyltransferaseC0023374
- Deficiency, Complete HPRTC0023374
- Deficiency, HGPRTC0023374
- Deficiency, Hypoxanthine PhosphoribosyltransferaseC0023374
- Deficiency, Total HPRTC0023374
- Guanine Phosphoribosyltransferase DeficienciesC0023374
- Guanine Phosphoribosyltransferase DeficiencyC0023374
- HGPRT DEFIC DIS COMPLETEC0023374
- HGPRT DeficienciesC0023374
- HGPRT DeficiencyC0023374
- HGPRT Deficiency Disease, CompleteC0023374
- HGPRT deficiencyC0023374
- HPRT - Hypoxanthine-guanine phosphoribosyltransferase deficiencyC0023374
- HPRT DEFICIENCYC0023374
- HPRT DEFICIENCY, COMPLETEC0023374
- HPRT Deficiencies, CompleteC0023374
- HPRT Deficiencies, TotalC0023374
- HPRT Deficiency, CompleteC0023374
- HPRT Deficiency, TotalC0023374
- HPRT1 DEFICIENCYC0023374
- HYPOXANTHINE GUANINE PHOSPHORIBOSYLTRANSFERASE 1 DEFICIENCYC0023374
- HYPOXANTHINE PHOSPHORIBOSYL TRANSFERASE DEFIC DISC0023374
- Hyperuricemia Syndrome, JuvenileC0023374
- Hyperuricemia Syndrome, PrimaryC0023374
- Hyperuricemia Syndromes, JuvenileC0023374
- Hyperuricemia Syndromes, PrimaryC0023374
- Hyperuricemia, X-LinkedC0023374
- Hyperuricemia, X-Linked PrimaryC0023374
- Hyperuricemias, X-LinkedC0023374
- Hyperuricemias, X-Linked PrimaryC0023374
- Hypoxanthine Guanine Phosphoribosyltransferase 1 DeficiencyC0023374
- Hypoxanthine Guanine Phosphoribosyltransferase DeficiencyC0023374
- Hypoxanthine Phosphoribosyl Transferase Deficiency DiseaseC0023374
- Hypoxanthine Phosphoribosyltransferase DeficienciesC0023374
- Hypoxanthine Phosphoribosyltransferase DeficiencyC0023374
- Hypoxanthine guanine phosphoribosyltransferase deficiencyC0023374
- Hypoxanthine phosphoribosyltransferase deficiencyC0023374
- Hypoxanthine-Phosphoribosyl-Transferase Deficiency DiseaseC0023374
- Hypoxanthine-Phosphoribosyl-Transferase Deficiency DiseasesC0023374
- Hypoxanthine-guanine phosphoribosyltransferase deficiencyC0023374
- Juvenile Gout, Choreoathetosis, Mental Retardation SyndromeC0023374
- Juvenile Hyperuricemia SyndromeC0023374
- Juvenile Hyperuricemia SyndromesC0023374
- Juvenile gout, choreoathetosis, mental retardation syndromeC0023374
- Juvenile hyperuricemia syndromeC0023374
- LESCH NYHAN DISC0023374
- LESCH-NYHAN SYNDROMEC0023374
- LNDC0023374
- LNSC0023374
- Lesch Nyhan DiseaseC0023374
- Lesch Nyhan SyndromeC0023374
- Lesch Nyhan syndromeC0023374
- Lesch-Nyhan DiseaseC0023374
- Lesch-Nyhan SyndromeC0023374
- Lesch-Nyhan diseaseC0023374
- Lesch-Nyhan syndromeC0023374
- Lesch-Nyhan syndrome (disorder)C0023374
- Phosphoribosyltransferase Deficiencies, GuanineC0023374
- Phosphoribosyltransferase Deficiencies, HypoxanthineC0023374
- Phosphoribosyltransferase Deficiency, GuanineC0023374
- Phosphoribosyltransferase Deficiency, HypoxanthineC0023374
- Primary Hyperuricemia SyndromeC0023374
- Primary Hyperuricemia SyndromesC0023374
- Primary Hyperuricemia, X-LinkedC0023374
- Primary Hyperuricemias, X-LinkedC0023374
- Primary hyperuricemia syndromeC0023374
- Self-Mutilation Syndrome, ChoreoathetosisC0023374
- Self-Mutilation Syndromes, ChoreoathetosisC0023374
- Syndrome, Choreoathetosis Self-MutilationC0023374
- Syndrome, Juvenile HyperuricemiaC0023374
- Syndrome, Primary HyperuricemiaC0023374
- Syndromes, Choreoathetosis Self-MutilationC0023374
- Syndromes, Juvenile HyperuricemiaC0023374
- Syndromes, Primary HyperuricemiaC0023374
- Total HGPRT deficiencyC0023374
- Total HPRT DeficienciesC0023374
- Total HPRT DeficiencyC0023374
- Total HPRT deficiencyC0023374
- Total Hypoxanthine Guanine Phosphoribosyl Transferase DeficiencyC0023374
- Total Hypoxanthine-Guanine Phosphoribosyl Transferase DeficiencyC0023374
- Total hypoxanthine-guanine phosphoribosyl transferase deficiencyC0023374
- X Linked HyperuricemiaC0023374
- X Linked Primary HyperuricemiaC0023374
- X-Linked HyperuricemiaC0023374
- X-Linked HyperuricemiasC0023374
- X-Linked Primary HyperuricemiaC0023374
- X-Linked Primary HyperuricemiasC0023374
- X-linked hyperuricaemiaC0023374
- X-linked hyperuricemiaC0023374
- X-linked primary hyperuricemiaC0023374
- X-linked uric aciduria enzyme defectC0023374
- lesch nyhan diseaseC0023374
- lesch nyhan syndromeC0023374
- lesch-nyhan diseaseC0023374
- lesch-nyhan syndromeC0023374
- nyhan syndromeC0023374
- nyhans syndromeC0023374
Frequently Asked Questions
What is the ICD-10 code for lesch-nyhan syndrome?
The ICD-10-CM code for lesch-nyhan syndrome is E79.1. The full clinical description is "Lesch-Nyhan syndrome". E79.1 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E79.1 mean?
ICD-10-CM code E79.1 represents "Lesch-Nyhan syndrome". 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 E79.1 a billable code?
Yes, E79.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E79.1 in?
E79.1 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E79.1?
E79.1 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 E79.1 map to?
E79.1 maps to 9 SNOMED CT concepts: 166735007, 269859006, 1259654009, 1259619002, 10406007, and 4 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E79.1?
E79.1 is linked to 1 UMLS Concept Unique Identifier: C0023374. 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.