Disorders of purine and pyrimidine metabolism E79-

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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)

Clinical Information

  • Condition in which there is a deviation or interruption in the processing of purine or pyrmidine in the body: its absorption, transport, storage, and utilization.

Codes

  • E79 Disorders of purine and pyrimidine metabolism
    •  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
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