E79.89
BillableOth disrd of purine and pyrimidine metabolism
Other specified disorders of purine and pyrimidine metabolism
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
- Congenital anomaly of macula4041005
- Hypouricaemia4519003
- Hypouricemia4519003
- ASase - Adenylosuccinate lyase deficiency15285008
- Adenylosuccinate deficiency15285008
- Adenylosuccinate lyase deficiency15285008
- Deficiency of adenylosuccinate lyase15285008
- Succinyladenosinuria15285008
- Succinylpurinaemic autism15285008
- Succinylpurinemic autism15285008
- Hereditary orotic aciduria16242007
- Hyperuricuria16813005
- Uricaciduria16813005
- Secondary orotic aciduria20155007
- BAIBA - beta-aminoisobutyric aciduria21529005
- Beta-aminoisobutyric aciduria21529005
- Deficiency of DNA repair28965003
- Deficiency of deoxyribonucleic acid repair28965003
- PRPPS overactivity35759001
- PRPS overactivity35759001
- Phosphoribosyl pyrophosphate synthase superactivity35759001
- Phosphoribosyl pyrophosphate synthetase overactivity35759001
- Ribose-phosphate pyrophosphokinase overactivity35759001
- Orotic aciduria47641009
- DNA repair65113001
- Deoxyribonucleic acid repair65113001
- APRT deficiency, Japanese type65791008
- Adenine phosphoribosyltransferase (APRT) deficiency, Japanese type65791008
- Adenine phosphoribosyltransferase deficiency, Japanese type65791008
- Combined orotic acid phosphoribosyltransferase and orotidine - 5 - phosphate decarboxylase deficiency69525003
- Hereditary orotic aciduria type 169525003
- Hereditary orotic aciduria, type 169525003
- OPRT AND OMP decarboxylase deficiency69525003
- Orotidylic pyrophosphorylase orotidylic decarboxylase deficiency69525003
- UMP synthase deficiency69525003
- UMPS - Uridine monophosphate synthase deficiency69525003
- Uridine monophosphate synthase deficiency69525003
- DPD - dihydropyrimidine dehydrogenase deficiency77365006
- Dihydropyrimidine dehydrogenase deficiency77365006
- Dihydrothymine dehydrogenase deficiency77365006
- Dihydrouracil dehydrogenase (NADP) deficiency77365006
- Dihydrouracil dehydrogenase (NADP^+^) deficiency77365006
- Dihydrouracil dehydrogenase (nicotinamide adenine dinucleotide phosphate ^+^) deficiency77365006
- Familial pyrimidinaemia77365006
- Familial pyrimidinemia77365006
- Hereditary thymine-uraciluria77365006
- Sensitivity to fluorouracil toxicity77365006
- Hereditary orotic aciduria type II90093009
- Hereditary orotic aciduria, type 290093009
- OMP decarboxylase deficiency90093009
- Orotidine-5'-phosphate decarboxylase deficiency90093009
- Orotidine-5-phosphate decarboxylase deficiency90093009
- Deficiency of hypoxanthine oxidase124147007
- Deficiency of xanthine oxidase124147007
- Xanthine oxidase deficiency124147007
- Deficiency of dihydrouracil dehydrogenase (NAD^+^)124163004
- Deficiency of dihydrouracil dehydrogenase (nicotinamide adenine dinucleotide ^+^)124163004
- Deficiency of phosphoribosylaminoimidazolecarboxamide formyltransferase124245006
- Deficiency of glycine formiminotransferase124246007
- Deficiency of aspartate carbamoyltransferase124248008
- Deficiency of aspartate transcarbamylase124248008
- Deficiency of carbamylaspartotranskinase124248008
- Deficiency of pyrimidine phosphorylase (uridine)124272003
- Deficiency of uridine phosphorylase124272003
- Deficiency of pyrimidine phosphorylase (thymidine)124273008
- Deficiency of thymidine phosphorylase124273008
- Adenine phosphoribosyl transferase deficiency124274002
- Deficiency of AMP pyrophorylase124274002
- Deficiency of adenine phosphoribosyltransferase124274002
- Deficiency of 5'-nucleotidase124434006
- Deficiency of 3'-nucleotidase124435007
- Deficiency of AMP nucleosidase124478002
- Deficiency of adenosine monophosphate nucleosidase124478002
- Deficiency of beta-ureidopropionase124511000
- Deficiency of allantoinase124517001
- Deficiency of allantoicase124519003
- Deficiency of adenase124521008
- Deficiency of adenine aminase124521008
- Deficiency of adenine deaminase124521008
- Deficiency of cytidine deaminase124524000
- Deficiency of AMP aminase124525004
- Deficiency of AMP deaminase124525004
- Deficiency of adenosine monophosphate deaminase124525004
- Deficiency of adenylic acid deaminase124525004
- Deficiency of trimetaphosphatase124530000
- Deficiency of phosphoribosylaminoimidazole carboxylase124597000
- Deficiency of phosphoribosylaminoimidazole-succinocarboxamide synthase124708004
- Deficiency of phosphoribosylaminoimidazole synthetase124709007
- Deficiency of phosphoribosylformylglycinamidine cyclo-ligase124709007
- Deficiency of GMP synthase (glutamine-hydrolysing)124714006
- Deficiency of GMP synthetase (glutamine-hydrolysing)124714006
- Deficiency of guanosine monophosphate synthase (glutamine-hydrolysing)124714006
- Deficiency of phosphoribosylformylglycinamidine synthase124715007
- Deficiency of phosphoribosylformylglycinamidine synthetase124715007
- Pyrimidine-5-nucleotidase deficiency234407001
- Uridine monophosphate hydrolase deficiency234407001
- Adenine phosphoribosyl transferase deficiency type I238009001
- Adenine phosphoribosyl transferase deficiency type II238010006
- ITPase - Inosine triphosphatase deficiency238011005
- Inosine triphosphate pyrophosphohydrolase deficiency238011005
- CDP - Cytosine diphosphate choline phosphotransferase deficiency238013008
- Cytosine diphosphate choline phosphotransferase deficiency238013008
- Dihydropyrimidinase deficiency238014002
- Dihydrouracil amidohydrolase deficiency238014002
- Phosphoribosyl pyrophosphate synthetase superactivity723454008
- Phosphoribosylpyrophosphate synthetase superactivity723454008
- 5-amino-4-imidazole carboxamide ribosiduria725289009
- AICA (5-amino-4-imidazole carboxamide) ribosiduria725289009
- ATIC (5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/imp cyclohydrolase) deficiency725289009
- Deficiency of nudix hydrolase 15781386002
- NUDT15 deficiency781386002
- Nucleotide diphosphatase deficiency781386002
- Thiopurine poor metaboliser 2781386002
- Thiopurine poor metabolizer 2781386002
- Deficiency of homologous recombination DNA (deoxyribonucleic acid) repair1255472001
- Deficiency of homologous recombination deoxyribonucleic acid repair1255472001
- Deficiency of homologous recombination repair1255472001
Frequently Asked Questions
What is the ICD-10 code for oth disrd of purine and pyrimidine metabolism?
The ICD-10-CM code for oth disrd of purine and pyrimidine metabolism is E79.89. The full clinical description is "Other specified disorders of purine and pyrimidine metabolism". E79.89 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E79.89 mean?
ICD-10-CM code E79.89 represents "Other specified disorders of purine and pyrimidine metabolism". 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 E79.89 a billable code?
Yes, E79.89 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E79.89 in?
E79.89 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E79.89?
E79.89 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 E79.89 map to?
E79.89 maps to 48 SNOMED CT concepts: 725289009, 65791008, 15285008, 124274002, 238009001, and 43 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E79.89?
E79.89 is linked to 1 UMLS Concept Unique Identifier: C5819111. 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.