Purine-Pyrimidine Metabolism, Inborn Errors

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

Year introduced: 1965

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Tree Number(s): C16.320.565.798, C18.452.648.798

MeSH Unique ID: D011686

Entry Terms:

• Purine Pyrimidine Metabolism, Inborn Errors

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Purine-Pyrimidine Metabolism, Inborn Errors
Dihydropyrimidine Dehydrogenase Deficiency
Gout
Arthritis, Gouty
Lesch-Nyhan Syndrome

All MeSH Categories
Diseases Category
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Purine-Pyrimidine Metabolism, Inborn Errors
Dihydropyrimidine Dehydrogenase Deficiency
Gout
Arthritis, Gouty
Lesch-Nyhan Syndrome