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- Dihydropyrimidine_dehydrogenase_deficiency abstract "Dihydropyrimidine dehydrogenase deficiency (DPD deficiency) is an autosomal recessivemetabolic disorder in which there is absent or significantly decreased activity of dihydropyrimidine dehydrogenase, an enzyme involved in the metabolism of uracil and thymine. Individuals with this condition may develop life-threatening toxicity following exposure to 5-fluorouracil (5-FU), a chemotherapy drug that is used in the treatment of cancer. Beside 5-FU, widely prescribed oral fluoropyrimidine capecitabine (Xeloda) could put DPD-deficient patients at risk of experiencing severe or lethal toxicities as well.".
- Dihydropyrimidine_dehydrogenase_deficiency diseasesdb "29817".
- Dihydropyrimidine_dehydrogenase_deficiency meshId "D054067".
- Dihydropyrimidine_dehydrogenase_deficiency omim "274270".
- Dihydropyrimidine_dehydrogenase_deficiency thumbnail Autorecessive.jpg?width=300.
- Dihydropyrimidine_dehydrogenase_deficiency wikiPageExternalLink dpd-deficiency.com.
- Dihydropyrimidine_dehydrogenase_deficiency wikiPageID "6061885".
- Dihydropyrimidine_dehydrogenase_deficiency wikiPageRevisionID "595651767".
- Dihydropyrimidine_dehydrogenase_deficiency diseasesdb "29817".
- Dihydropyrimidine_dehydrogenase_deficiency hasPhotoCollection Dihydropyrimidine_dehydrogenase_deficiency.
- Dihydropyrimidine_dehydrogenase_deficiency meshid "D054067".
- Dihydropyrimidine_dehydrogenase_deficiency name "Dihydropyrimidine dehydrogenase deficiency".
- Dihydropyrimidine_dehydrogenase_deficiency omim "274270".
- Dihydropyrimidine_dehydrogenase_deficiency wordnet_type synset-disease-noun-1.
- Dihydropyrimidine_dehydrogenase_deficiency subject Category:Autosomal_recessive_disorders.
- Dihydropyrimidine_dehydrogenase_deficiency subject Category:Inborn_errors_of_purine-pyrimidine_metabolism.
- Dihydropyrimidine_dehydrogenase_deficiency type Abstraction100002137.
- Dihydropyrimidine_dehydrogenase_deficiency type Act100030358.
- Dihydropyrimidine_dehydrogenase_deficiency type Attribute100024264.
- Dihydropyrimidine_dehydrogenase_deficiency type AutosomalRecessiveDisorders.
- Dihydropyrimidine_dehydrogenase_deficiency type Condition113920835.
- Dihydropyrimidine_dehydrogenase_deficiency type Disease114070360.
- Dihydropyrimidine_dehydrogenase_deficiency type Disorder114052403.
- Dihydropyrimidine_dehydrogenase_deficiency type Event100029378.
- Dihydropyrimidine_dehydrogenase_deficiency type IllHealth114052046.
- Dihydropyrimidine_dehydrogenase_deficiency type Illness114061805.
- Dihydropyrimidine_dehydrogenase_deficiency type InbornErrorsOfMetabolism.
- Dihydropyrimidine_dehydrogenase_deficiency type InbornErrorsOfPurine-pyrimidineMetabolism.
- Dihydropyrimidine_dehydrogenase_deficiency type Mistake100070965.
- Dihydropyrimidine_dehydrogenase_deficiency type Nonaccomplishment100066216.
- Dihydropyrimidine_dehydrogenase_deficiency type PathologicalState114051917.
- Dihydropyrimidine_dehydrogenase_deficiency type PhysicalCondition114034177.
- Dihydropyrimidine_dehydrogenase_deficiency type PsychologicalFeature100023100.
- Dihydropyrimidine_dehydrogenase_deficiency type State100024720.
- Dihydropyrimidine_dehydrogenase_deficiency type YagoPermanentlyLocatedEntity.
- Dihydropyrimidine_dehydrogenase_deficiency type Disease.
- Dihydropyrimidine_dehydrogenase_deficiency type AilmentCondition.
- Dihydropyrimidine_dehydrogenase_deficiency type Situation.
- Dihydropyrimidine_dehydrogenase_deficiency comment "Dihydropyrimidine dehydrogenase deficiency (DPD deficiency) is an autosomal recessivemetabolic disorder in which there is absent or significantly decreased activity of dihydropyrimidine dehydrogenase, an enzyme involved in the metabolism of uracil and thymine. Individuals with this condition may develop life-threatening toxicity following exposure to 5-fluorouracil (5-FU), a chemotherapy drug that is used in the treatment of cancer.".
- Dihydropyrimidine_dehydrogenase_deficiency label "Dihydropyrimidine dehydrogenase deficiency".
- Dihydropyrimidine_dehydrogenase_deficiency sameAs m.0fn4rd.
- Dihydropyrimidine_dehydrogenase_deficiency sameAs Q5276448.
- Dihydropyrimidine_dehydrogenase_deficiency sameAs Q5276448.
- Dihydropyrimidine_dehydrogenase_deficiency sameAs Dihydropyrimidine_dehydrogenase_deficiency.
- Dihydropyrimidine_dehydrogenase_deficiency wasDerivedFrom Dihydropyrimidine_dehydrogenase_deficiency?oldid=595651767.
- Dihydropyrimidine_dehydrogenase_deficiency depiction Autorecessive.jpg.
- Dihydropyrimidine_dehydrogenase_deficiency isPrimaryTopicOf Dihydropyrimidine_dehydrogenase_deficiency.
- Dihydropyrimidine_dehydrogenase_deficiency name "Dihydropyrimidine dehydrogenase deficiency".