Dihydropyrimidine dehydrogenase deficiency   77365006

SNOMED CT code


SNOMED code77365006
nameDihydropyrimidine dehydrogenase deficiency
statusactive
date introduced2002-01-31
fully specified name(s)Dihydropyrimidine dehydrogenase deficiency (disorder)
synonyms
  • Dihydrouracil dehydrogenase (NADP^+^) deficiency
  • Dihydropyrimidine dehydrogenase deficiency
  • Dihydrothymine dehydrogenase deficiency
  • Sensitivity to fluorouracil toxicity
  • Hereditary thymine-uraciluria
  • Familial pyrimidinemia
  • Dihydrouracil dehydrogenase (nicotinamide adenine dinucleotide phosphate ^+^) deficiency
  • DPD - dihydropyrimidine dehydrogenase deficiency
  • Dihydrouracil dehydrogenase (NADP) deficiency
  • Familial pyrimidinaemia
parents
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Enzymopathy   78548001
          Dihydropyrimidine dehydrogenase deficiency   77365006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Disorder of pyrimidine metabolism   85444005
          Dihydropyrimidine dehydrogenase deficiency   77365006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Dihydropyrimidine dehydrogenase deficiency   77365006

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