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

No definition found.

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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