Category: E79 - Disorders of purine and pyrimidine metabolism

 Chapter Notes

 Section Notes

 E79

Disorders of purine and pyrimidine metabolism

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)

 E79.0

Hyperuricemia without signs of inflammatory arthritis and tophaceous disease

Asymptomatic hyperuricemia

 E79.1

Lesch-Nyhan syndrome

HGPRT deficiency

 E79.2

Myoadenylate deaminase deficiency

 E79.8

Other disorders of purine and pyrimidine metabolism

Hereditary xanthinuria

 E79.9

Disorder of purine and pyrimidine metabolism, unspecified