Disease: Coumarin Sensitivity ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2675747
Disease: Coumarin Sensitivity
Coumarin Sensitivity 		0.020 GeneticVariation phenotype BEFREE Homozygous carriers of the VKORC1*2 allele are strongly predisposed to coumarin sensitivity. 17849045 2007
CUI: C2675747
Disease: Coumarin Sensitivity
Coumarin Sensitivity 		0.020 GeneticVariation phenotype BEFREE A C1173T dimorphism in the VKORC1 gene determines coumarin sensitivity and bleeding risk. 16201835 2005