dihydropyrimidine dehydrogenase deficiency Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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://www.omim.org/entry/274270
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Genes

1 genes associated with the dihydropyrimidine dehydrogenase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
DPYD dihydropyrimidine dehydrogenase