Disorders of purine and pyrimidine metabolism - E79
Excludes1: It indicates that the conditions described by two codes cannot occur together in the same patient. These codes are mutually exclusive.
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)
These ranges represents subcategories of Disorders of purine and pyrimidine metabolism. The "E79" signifies that these are the diseases within this broad category.
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