dihydropyrimidine dehydrogenase deficiency (Q5276448)
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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
| Language | Label | Description | Also known as |
|---|---|---|---|
| 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 |
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Identifiers
Dihydropyrimidine Dehydrogenase Deficiency
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