Source: UNIPROT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7450
Gene Symbol: VWF
VWF
CUI: C1264040
Disease: von Willebrand Disease, Type 2
von Willebrand Disease, Type 2 		1.000 GeneticVariation UNIPROT The molecular defect in type IIB von Willebrand disease. Identification of four potential missense mutations within the putative GpIb binding domain. 1672694

1991
Entrez Id: 7450
Gene Symbol: VWF
VWF
CUI: C1264040
Disease: von Willebrand Disease, Type 2
von Willebrand Disease, Type 2 		1.000 GeneticVariation UNIPROT Analysis of the relationship of von Willebrand disease (vWD) and hereditary hemorrhagic telangiectasia and identification of a potential type IIA vWD mutation (IIe865 to Thr). 1673047

1991
Entrez Id: 7450
Gene Symbol: VWF
VWF
CUI: C1264040
Disease: von Willebrand Disease, Type 2
von Willebrand Disease, Type 2 		1.000 GeneticVariation UNIPROT An Arg545----Cys545 substitution mutation of the von Willebrand factor in type IIB von Willebrand's disease. 1761120

1991
Entrez Id: 7450
Gene Symbol: VWF
VWF
CUI: C1264040
Disease: von Willebrand Disease, Type 2
von Willebrand Disease, Type 2 		1.000 GeneticVariation UNIPROT Molecular basis of human von Willebrand disease: analysis of platelet von Willebrand factor mRNA. 2786201

1989