Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Metabolism, Inborn Errors » Purine-Pyrimidine Metabolism, Inborn Errors
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Metabolism, Inborn Errors » Purine-Pyrimidine Metabolism, Inborn Errors
Description
Dysfunctions in the metabolism of PURINES or PYRIMIDINES resulting from inborn genetic mutations that are inherited or acquired in utero. MeSH
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Subtype Terms (3)
Gout
105 drugs (61 approved, 44 experimental)
Lesch-Nyhan Syndrome
2 drugs (1 approved, 1 experimental)
Organization Involved with Phase 2 Indications (2)
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