Congenital Disorder

Purine-Pyrimidine Metabolism, Inborn Errors

AMW:DIS:160134

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

Pathology clinical

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Purine-Pyrimidine Metabolism, Inborn Errors has parent Metabolism, Inborn Errors

Gout has parent Purine-Pyrimidine Metabolism, Inborn Errors

Lesch-Nyhan Syndrome has parent Purine-Pyrimidine Metabolism, Inborn Errors

Dihydropyrimidine Dehydrogenase Deficiency has parent Purine-Pyrimidine Metabolism, Inborn Errors

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