Disorders of purine and pyrimidine metabolism - E79

 Type 1 Excludes

  • 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)

 Codes

  • E79.0 - Hyperuricemia without signs of inflammatory arthritis and tophaceous disease
  • E79.1 - Lesch-Nyhan syndrome
  • E79.2 - Myoadenylate deaminase deficiency
  • E79.8 - Other disorders of purine and pyrimidine metabolism
  • E79.81 - Aicardi-Goutières syndrome
  • E79.82 - Hereditary xanthinuria
  • E79.89 - Other specified disorders of purine and pyrimidine metabolism
  • E79.9 - Disorder of purine and pyrimidine metabolism, unspecified