Purine-Pyrimidine Metabolism, Inborn Errors

"Purine-Pyrimidine Metabolism, Inborn Errors" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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

Descriptor ID	D011686
MeSH Number(s)	C16.320.565.798 C18.452.648.798
Concept/Terms	Purine-Pyrimidine Metabolism, Inborn Errors Purine-Pyrimidine Metabolism, Inborn Errors Purine Pyrimidine Metabolism, Inborn Errors

Below are MeSH descriptors whose meaning is more general than "Purine-Pyrimidine Metabolism, Inborn Errors".

Diseases [C]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Metabolism, Inborn Errors [C16.320.565]
Purine-Pyrimidine Metabolism, Inborn Errors [C16.320.565.798]
Nutritional and Metabolic Diseases [C18]
Metabolic Diseases [C18.452]
Metabolism, Inborn Errors [C18.452.648]
Purine-Pyrimidine Metabolism, Inborn Errors [C18.452.648.798]

Below are MeSH descriptors whose meaning is related to "Purine-Pyrimidine Metabolism, Inborn Errors".

Below are MeSH descriptors whose meaning is more specific than "Purine-Pyrimidine Metabolism, Inborn Errors".

Purine-Pyrimidine Metabolism, Inborn Errors
Dihydropyrimidine Dehydrogenase Deficiency
Gout
Lesch-Nyhan Syndrome

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