dihydropyrimidine dehydrogenase deficiency Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description 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. (Human Disease Ontology, DOID_14218)
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1 genes associated with the disease dihydropyrimidine dehydrogenase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
DPYD dihydropyrimidine dehydrogenase