Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C1282971
Disease: von Willebrand Disease, Type 2B
von Willebrand Disease, Type 2B 		8 0 4 0.50 0 0
CUI: C0472801
Disease: Hemophilia A carrier
Hemophilia A carrier 		3 0 2 0.40 0 0
CUI: C1282974
Disease: von Willebrand disease type 2M
von Willebrand disease type 2M 		3 0 2 0.40 0 0
CUI: C0272323
Disease: Moderate hereditary factor VIII deficiency disease
Moderate hereditary factor VIII deficiency disease 		4 0 2 0.33 0 0
CUI: C1280798
Disease: Von Willebrand disease, platelet type
Von Willebrand disease, platelet type 		8 0 3 0.33 0 0
CUI: C3641106
Disease: Congenital Bleeding Disorder
Congenital Bleeding Disorder 		4 0 2 0.33 0 0
CUI: C0017145
Disease: Gastric Varix
Gastric Varix 		5 0 2 0.29 0 0
CUI: C0272328
Disease: Acquired factor X deficiency disease
Acquired factor X deficiency disease 		1 0 1 0.25 0 0
CUI: C0272355
Disease: von Willebrand disease, type IIC
von Willebrand disease, type IIC 		1 0 1 0.25 0 0
CUI: C0272356
Disease: von Willebrand disease, type IID
von Willebrand disease, type IID 		1 0 1 0.25 0 0
CUI: C0333183
Disease: Partial stenosis
Partial stenosis 		1 0 1 0.25 0 0
CUI: C0398610
Disease: Congenital von Willebrand's disease
Congenital von Willebrand's disease 		1 0 1 0.25 0 0
CUI: C0598480
Disease: intestinal angiodysplasia
intestinal angiodysplasia 		1 0 1 0.25 0 0
CUI: C0795843
Disease: Chromosome 12 ring
Chromosome 12 ring 		1 0 1 0.25 0 0
CUI: C0865262
Disease: Thrombopathy
Thrombopathy 		1 0 1 0.25 0 0
CUI: C0877456
Disease: Heyde's syndrome
Heyde's syndrome 		1 0 1 0.25 0 0
CUI: C1264040
Disease: von Willebrand Disease, Type 2
von Willebrand Disease, Type 2 		6 39 2 0.25 11 0.24
CUI: C1266156
Disease: Multicystic mesothelioma, benign
Multicystic mesothelioma, benign 		1 0 1 0.25 0 0
CUI: C1848525
Disease: von Willebrand Disease, Recessive Form
von Willebrand Disease, Recessive Form 		1 0 1 0.25 0 0
CUI: C2584751
Disease: Severe hereditary factor VIII deficiency disease without inhibitor
Severe hereditary factor VIII deficiency disease without inhibitor 		1 0 1 0.25 0 0
CUI: C2584777
Disease: Autoimmune thrombotic thrombocytopenic purpura
Autoimmune thrombotic thrombocytopenic purpura 		1 0 1 0.25 0 0
CUI: C4017296
Disease: VON WILLEBRAND DISEASE, TYPE 1, SUSCEPTIBILITY TO
VON WILLEBRAND DISEASE, TYPE 1, SUSCEPTIBILITY TO 		1 0 1 0.25 0 0
CUI: C4017650
Disease: VON WILLEBRAND FACTOR VICENZA PHENOTYPE
VON WILLEBRAND FACTOR VICENZA PHENOTYPE 		1 0 1 0.25 0 0
CUI: C4321502
Disease: Factor XI Deficiency
Factor XI Deficiency 		6 0 2 0.25 0 0
CUI: C4728230
Disease: Capnocytophaga canimorsus sepsis
Capnocytophaga canimorsus sepsis 		1 0 1 0.25 0 0