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E792026

Non-billable

Disorders of purine and pyrimidine metabolism

Clinical Notes

  • 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)
From E70-E88
  • 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)
From E00-E89
  • Transitory endocrine and metabolic disorders specific to newborn (P70-P74)

Frequently Asked Questions

Code Hierarchy
E79
Disorders of purine and pyrimidine metabolism
Hyperuricemia without signs of inflammatory arthritis and tophaceous disease
Lesch-Nyhan syndrome
Myoadenylate deaminase deficiency
Other disorders of purine and pyrimidine metabolism
Disorder of purine and pyrimidine metabolism, unspecified

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Related MS-DRGs
34,719 Medicare hospitalizations across 3 DRGs for codes in E79

Top DRGs associated with codes in this category:

948SIGNS AND SYMPTOMS WITHOUT MCC18,393
642INBORN AND OTHER DISORDERS OF METABOLISM9,780
947SIGNS AND SYMPTOMS WITH MCC6,546
Official Guidelines
Chapter 4: Endocrine, Nutritional, and Metabolic Diseases

Official coding guidelines for E00-E89

Disorders of purine and pyrimidine metabolism - ICD-10 Code E79 | FindICD10