Dihydropyrimidine Dehydrogenase Deficiency Gene Set

Dataset CTD 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)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D054067
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1 genes/proteins associated with the disease Dihydropyrimidine Dehydrogenase Deficiency from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
DPYD dihydropyrimidine dehydrogenase 2.88009