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: C0272362
Disease: Acquired von Willebrand's disease
Acquired von Willebrand's disease 		8 0 2 0.17 0 0
CUI: C0333183
Disease: Partial stenosis
Partial stenosis 		1 0 1 0.17 0 0
CUI: C0398610
Disease: Congenital von Willebrand's disease
Congenital von Willebrand's disease 		1 0 1 0.17 0 0
CUI: C0585110
Disease: Hemorrhagic pleural effusion
Hemorrhagic pleural effusion 		1 0 1 0.17 0 0
CUI: C0598480
Disease: intestinal angiodysplasia
intestinal angiodysplasia 		1 0 1 0.17 0 0
CUI: C0795843
Disease: Chromosome 12 ring
Chromosome 12 ring 		1 0 1 0.17 0 0
CUI: C0865262
Disease: Thrombopathy
Thrombopathy 		1 0 1 0.17 0 0
CUI: C0877456
Disease: Heyde's syndrome
Heyde's syndrome 		1 0 1 0.17 0 0
CUI: C1266156
Disease: Multicystic mesothelioma, benign
Multicystic mesothelioma, benign 		1 0 1 0.17 0 0
CUI: C1848525
Disease: von Willebrand Disease, Recessive Form
von Willebrand Disease, Recessive Form 		1 4 1 0.17 1 2.4E-02
CUI: C2584751
Disease: Severe hereditary factor VIII deficiency disease without inhibitor
Severe hereditary factor VIII deficiency disease without inhibitor 		1 0 1 0.17 0 0
CUI: C3890932
Disease: FACTOR VIII (OKAYAMA) PHENOTYPE
FACTOR VIII (OKAYAMA) PHENOTYPE 		1 0 1 0.17 0 0
CUI: C3900057
Disease: Allograft Thrombosis
Allograft Thrombosis 		1 0 1 0.17 0 0
CUI: C4017296
Disease: VON WILLEBRAND DISEASE, TYPE 1, SUSCEPTIBILITY TO
VON WILLEBRAND DISEASE, TYPE 1, SUSCEPTIBILITY TO 		1 0 1 0.17 0 0
CUI: C4017565
Disease: FACTOR VIII (EAST HARTFORD) PHENOTYPE
FACTOR VIII (EAST HARTFORD) PHENOTYPE 		1 0 1 0.17 0 0
CUI: C4017650
Disease: VON WILLEBRAND FACTOR VICENZA PHENOTYPE
VON WILLEBRAND FACTOR VICENZA PHENOTYPE 		1 0 1 0.17 0 0
CUI: C1844374
Disease: Persistent bleeding after trauma
Persistent bleeding after trauma 		9 0 2 0.15 0 0
CUI: C0263675
Disease: Chronic arthropathy
Chronic arthropathy 		2 0 1 0.14 0 0
CUI: C0266604
Disease: Congenital aplasia of inner ear
Congenital aplasia of inner ear 		2 0 1 0.14 0 0
CUI: C0333203
Disease: Occlusive thrombus
Occlusive thrombus 		2 0 1 0.14 0 0
CUI: C0542259
Disease: Morphological abnormality of the vestibule of the inner ear
Morphological abnormality of the vestibule of the inner ear 		2 0 1 0.14 0 0
CUI: C0574027
Disease: Vertebral artery aneurysm
Vertebral artery aneurysm 		2 0 1 0.14 0 0
CUI: C1096487
Disease: Hereditary factor VIII deficiency disease without inhibitor
Hereditary factor VIII deficiency disease without inhibitor 		2 0 1 0.14 0 0
CUI: C1853162
Disease: Osteogenesis Imperfecta Type VII
Osteogenesis Imperfecta Type VII 		2 0 1 0.14 0 0
CUI: C3494186
Disease: Autosomal Hemophilia A
Autosomal Hemophilia A 		2 0 1 0.14 0 0