Compound: FDB002253 (3-Aminopropanoic acid)
Term: Dihydropyrimidine dehydrogenase deficiency
Definition: A purine-pyrimidine metabolic disorder that is an autosomal recessive metabolic disorder in which there is absent or significantly decreased activity of dihydropyrimidine dehydrogenase, an enzyme involved in the metabolism of uracil and thymine. (do).
Parent Term: Metabolism and nutrition disorders
Parent Definition: A group of disorders, inherited or not, that result in a metabolic malfunction.
Synonyms
Other Compounds Mapped to 'Dihydropyrimidine dehydrogenase deficiency'