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Statements

Subject Item
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dbpedia:Dihydropyrimidine_dehydrogenase_deficiency
schema:description
хвороба Krankheit 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 maladie
p:P2888
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p:P1995
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DOID:14218
rdfs:label
DPD欠損症 dihydropyrimidine dehydrogenase deficiency Dihydropyrimidin-Dehydrogenase-Mangel déficit en dihydropyrimidine déshydrogénase کمبود دی هیدروپیریمیدین دهیدروژناز
skos:prefLabel
کمبود دی هیدروپیریمیدین دهیدروژناز Dihydropyrimidin-Dehydrogenase-Mangel dihydropyrimidine dehydrogenase deficiency déficit en dihydropyrimidine déshydrogénase DPD欠損症
schema:name
déficit en dihydropyrimidine déshydrogénase DPD欠損症 dihydropyrimidine dehydrogenase deficiency Dihydropyrimidin-Dehydrogenase-Mangel کمبود دی هیدروپیریمیدین دهیدروژناز
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p:P7464
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wdt:P11430
DI-01488
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1675
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277.2
wdt:P2293
wd:Q18022858
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dihydropyrimidine-dehydrogenase-deficiency
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dihydropyrimidine-dehydrogenase-deficiency
p:P3841
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HP:0003654
skos:altLabel
thymine-uracilurea 5-Fluorouracil Toxicity Familial pyrimidinemia Thymine-Uraciluria, Hereditary Dpd Deficiency Hereditary thymine-uraciluria Dpyd Deficiency Dihydropyrimidine dehydrogenase deficiency Dihydropyrimidine dehydrogenase deficiency (disorder) Pyrimidinemia, Familial familial pyrimidinaemia Dihydrouracil Dehydrogenase deficiency
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C3964 C84672
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C3495551 C1959620 C4025582 C2720286 C0274576
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D054067
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Dihydropyrimidine dehydrogenase deficiency