inborn error of purine-pyrimidine metabolism pathway
dihydropyrimidine dehydrogenase deficiency pathway
2015-11-10T10:22:12Z
An autosomal recessive disorder resulting from alterations in pyrimidine degradation pathway due to mutations in dihydropyrimidine gene (DPYD). DPYD catalyzes the initial and rate-limiting step in pyrimidine bases (uracil and thymine) catabolism.
PW:0002210
SMP:00179
VPetri
pathway