Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Deficiencies, Dihydropyrimidine Dehydrogenase DPYD disease C1959620 GeneticVariation 0.8 orphanet , disgenet
Deficiencies, Dihydropyrimidine Dehydrogenase DPYD disease C1959620 Biomarker 0.8 orphanet , disgenet
Deficiencies, Dihydropyrimidine Dehydrogenase DPYD disease C1959620 AlteredExpression 0.8 orphanet , disgenet
Deficiencies, Dihydropyrimidine Dehydrogenase DPYD disease C1959620 PosttranslationalModification 0.8 orphanet , disgenet
Deficiencies, Dihydropyrimidine Dehydrogenase DPYD disease C1959620 GermlineCausalMutation 0.8 orphanet , disgenet
Deficiencies, Dihydropyrimidine Dehydrogenase DPYD disease C1959620 CausalMutation 0.8 orphanet , disgenet
Deficiencies, Dihydropyrimidine Dehydrogenase TYMS disease C1959620 Biomarker 0.02 disgenet
Deficiencies, Dihydropyrimidine Dehydrogenase TYMS disease C1959620 GeneticVariation 0.02 disgenet
Deficiencies, Dihydropyrimidine Dehydrogenase FANCD2 disease C1959620 GeneticVariation 0.01 disgenet
Deficiencies, Dihydropyrimidine Dehydrogenase ANIB1 disease C1959620 Biomarker 0.01 disgenet
Deficiencies, Dihydropyrimidine Dehydrogenase PSEN1 disease C1959620 GeneticVariation 0.01 disgenet
Deficiencies, Dihydropyrimidine Dehydrogenase BRCA2 disease C1959620 GeneticVariation 0.01 disgenet
Deficiencies, Dihydropyrimidine Dehydrogenase EDIL3 disease C1959620 GeneticVariation 0.01 disgenet
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