E79.8

Other disorders of purine and pyrimidine metabolism

Coding guidance (WHO 2019)

Hereditary xanthinuria

Sibling codes

E79Disorders of purine and pyrimidine metabolism E79.0Hyperuricaemia without signs of inflammatory arthritis and tophaceous disease E79.1Lesch-Nyhan syndrome E79.9Disorder of purine and pyrimidine metabolism, unspecified

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