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: 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: C1282968
Disease: von Willebrand Disease, Type 2A
von Willebrand Disease, Type 2A 		4 0 2 0.33 0 0
CUI: C1282971
Disease: von Willebrand Disease, Type 2B
von Willebrand Disease, Type 2B 		8 0 3 0.33 0 0
CUI: C4025649
Disease: Reduced factor VIII activity
Reduced factor VIII activity 		4 0 2 0.33 0 0
CUI: C0151445
Disease: Primary Raynaud Phenomenon
Primary Raynaud Phenomenon 		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: C0272343
Disease: Familial multiple factor deficiency syndrome, type II
Familial multiple factor deficiency syndrome, type II 		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: C0341012
Disease: Oral herpes simplex infection
Oral herpes simplex infection 		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: C0585110
Disease: Hemorrhagic pleural effusion
Hemorrhagic pleural effusion 		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 0 2 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: C3890932
Disease: FACTOR VIII (OKAYAMA) PHENOTYPE
FACTOR VIII (OKAYAMA) PHENOTYPE 		1 0 1 0.25 0 0
CUI: C3900057
Disease: Allograft Thrombosis
Allograft Thrombosis 		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: C4017565
Disease: FACTOR VIII (EAST HARTFORD) PHENOTYPE
FACTOR VIII (EAST HARTFORD) PHENOTYPE 		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