E79 Disorders of purine and pyrimidine metabolism

Non-Billable/Non-Specific

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

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