AutoICD API

E79.89

Billable

Oth disrd of purine and pyrimidine metabolism

Other specified disorders of purine and pyrimidine metabolism

Status

Billable / Specific

Block

E70-E88

Parent Code

E79.8

Coding Notes

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(2)
E79.81

Aicardi-Goutieres syndrome

BillableE79.82

Hereditary xanthinuria

Billable
Also Known As / Clinical Terms(236)

SNOMED CT

UMLS

Clinical Terms

  • Adenine phosphoribosyl transferase deficiency type I
  • Deficiency of trimetaphosphatase
  • Sensitivity to fluorouracil toxicity
  • Thiopurine poor metabolizer 2
  • Deficiency of 5'-nucleotidase
  • Deficiency of xanthine oxidase
  • Deficiency of GMP synthase (glutamine-hydrolysing)
  • Deficiency of phosphoribosylaminoimidazolecarboxamide formyltransferase
  • Adenine phosphoribosyltransferase (APRT) deficiency, Japanese type
  • 5-amino-4-imidazole carboxamide ribosiduria
  • Deficiency of homologous recombination deoxyribonucleic acid repair
  • Pyrimidine-5-nucleotidase deficiency
  • Deficiency of cytidine deaminase
  • Deficiency of glycine formiminotransferase
  • Secondary orotic aciduria
  • Hypouricaemia
  • Deficiency of aspartate transcarbamylase
  • Phosphoribosyl pyrophosphate synthetase overactivity
  • Hereditary orotic aciduria, type 2
  • Inosine triphosphate pyrophosphohydrolase deficiency
  • Hyperuricuria
  • Dihydropyrimidine dehydrogenase deficiency
  • Congenital anomaly of macula
  • Dihydrouracil dehydrogenase (NADP^+^) deficiency
  • Deficiency of allantoinase
  • Deficiency of homologous recombination repair
  • Deficiency of guanosine monophosphate synthase (glutamine-hydrolysing)
  • CDP - Cytosine diphosphate choline phosphotransferase deficiency
  • APRT deficiency, Japanese type
  • PRPS overactivity
  • Deficiency of phosphoribosylaminoimidazole-succinocarboxamide synthase
  • Deficiency of pyrimidine phosphorylase (thymidine)
  • Deficiency of homologous recombination DNA (deoxyribonucleic acid) repair
  • Deficiency of adenylic acid deaminase
  • Succinyladenosinuria
  • BAIBA - beta-aminoisobutyric aciduria
  • Succinylpurinaemic autism
  • Deficiency of nudix hydrolase 15
  • Deficiency of aspartate carbamoyltransferase
  • OMP decarboxylase deficiency
  • Deficiency of DNA repair
  • Adenylosuccinate deficiency
  • Dihydrothymine dehydrogenase deficiency
  • Adenine phosphoribosyl transferase deficiency type II
  • Beta-aminoisobutyric aciduria
  • Nucleotide diphosphatase deficiency
  • Deficiency of phosphoribosylaminoimidazole synthetase
  • Orotidylic pyrophosphorylase orotidylic decarboxylase deficiency
  • Adenylosuccinate lyase deficiency
  • Orotidine-5-phosphate decarboxylase deficiency
  • Deficiency of adenase
  • Familial pyrimidinemia
  • Familial pyrimidinaemia
  • Deficiency of beta-ureidopropionase
  • Deficiency of AMP pyrophorylase
  • Deficiency of pyrimidine phosphorylase (uridine)
  • Uricaciduria
  • Phosphoribosyl pyrophosphate synthase superactivity
  • Uridine monophosphate hydrolase deficiency
  • Dihydrouracil dehydrogenase (nicotinamide adenine dinucleotide phosphate ^+^) deficiency
  • Hereditary orotic aciduria type II
  • Phosphoribosylpyrophosphate synthetase superactivity
  • Deficiency of thymidine phosphorylase
  • Deficiency of phosphoribosylformylglycinamidine synthetase
  • Adenine phosphoribosyl transferase deficiency
  • Deficiency of hypoxanthine oxidase
  • Hereditary orotic aciduria type 1
  • Deficiency of AMP deaminase
  • NUDT15 deficiency
  • Hereditary orotic aciduria
  • Cytosine diphosphate choline phosphotransferase deficiency
  • Dihydrouracil amidohydrolase deficiency
  • Deficiency of adenine deaminase
  • Uridine monophosphate synthase deficiency
  • Deficiency of phosphoribosylformylglycinamidine synthase
  • Deficiency of phosphoribosylformylglycinamidine cyclo-ligase
  • Deficiency of allantoicase
  • ASase - Adenylosuccinate lyase deficiency
  • Hypouricemia
  • OPRT AND OMP decarboxylase deficiency
  • Deficiency of carbamylaspartotranskinase
  • ATIC (5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/imp cyclohydrolase) deficiency
  • PRPPS overactivity
  • Dihydropyrimidinase deficiency
  • Deficiency of AMP nucleosidase
  • Deficiency of dihydrouracil dehydrogenase (NAD^+^)
  • Combined orotic acid phosphoribosyltransferase and orotidine - 5 - phosphate decarboxylase deficiency
  • Deficiency of adenine aminase
  • UMPS - Uridine monophosphate synthase deficiency
  • DNA repair
  • AICA (5-amino-4-imidazole carboxamide) ribosiduria
  • Deficiency of phosphoribosylaminoimidazole carboxylase
  • Deficiency of dihydrouracil dehydrogenase (nicotinamide adenine dinucleotide ^+^)
  • Deficiency of adenylosuccinate lyase
  • Thiopurine poor metaboliser 2
  • Deficiency of adenine phosphoribosyltransferase
  • ITPase - Inosine triphosphatase deficiency
  • Deficiency of adenosine monophosphate deaminase
  • Deficiency of 3'-nucleotidase
  • UMP synthase deficiency
  • Succinylpurinemic autism
  • Hereditary thymine-uraciluria
  • Adenine phosphoribosyltransferase deficiency, Japanese type
  • Xanthine oxidase deficiency
  • Deficiency of AMP aminase
  • Deoxyribonucleic acid repair
  • Hereditary orotic aciduria, type 1
  • Deficiency of uridine phosphorylase
  • Dihydrouracil dehydrogenase (NADP) deficiency
  • Phosphoribosyl pyrophosphate synthetase superactivity
  • Orotidine-5'-phosphate decarboxylase deficiency
  • Deficiency of GMP synthetase (glutamine-hydrolysing)
  • Orotic aciduria
  • Ribose-phosphate pyrophosphokinase overactivity
  • Deficiency of adenosine monophosphate nucleosidase
  • DPD - dihydropyrimidine dehydrogenase deficiency
  • Deficiency of deoxyribonucleic acid repair
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.

How does E79.89 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like oth disrd of purine and pyrimidine metabolism 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 E79.89?

There is no direct ICD-11 mapping available for E79.89 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.