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Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Purine-Pyrimidine Metabolism, Inborn Errors
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Purine-Pyrimidine Metabolism, Inborn Errors

Preferred term

Purine-Pyrimidine Metabolism, Inborn Errors  

Type

  • Topical Descriptor

Broader concept

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Entry terms

  • Purine Pyrimidine Metabolism, Inborn Errors

Note

  • coordinate with specific purine /metab or pyrimidine /metab

Scope note

  • Dysfunctions in the metabolism of PURINES or PYRIMIDINES resulting from inborn genetic mutations that are inherited or acquired in utero.

History note

  • 65

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URI

http://www.yso.fi/onto/mesh/D011686

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