(Q5276448)
English
dihydropyrimidine dehydrogenase deficiency
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
- Dihydropyrimidine dehydrogenase deficiency (disorder)
- Dihydrouracil Dehydrogenase deficiency
- familial pyrimidinaemia
- thymine-uracilurea
- Dihydropyrimidine dehydrogenase deficiency
- Familial pyrimidinemia
- Dpyd Deficiency
- 5-Fluorouracil Toxicity
- Thymine-Uraciluria, Hereditary
- Pyrimidinemia, Familial
- Dpd Deficiency
- Hereditary thymine-uraciluria
Statements
1 reference
1 reference
1 reference
3 references
277.2
1 reference
1 reference
1 reference
Identifiers
Dihydropyrimidine Dehydrogenase Deficiency
1 reference
1 reference
2 references
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
2 references
1 reference