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: C0936263
Disease: Cerebral Thrombus
Cerebral Thrombus 		3 0 3 1.00 0 0
CUI: C0936261
Disease: Brain Thrombus
Brain Thrombus 		5 0 3 0.60 0 0
CUI: C0752143
Disease: Intracranial Thrombosis
Intracranial Thrombosis 		6 0 3 0.50 0 0
CUI: C0085307
Disease: Embolism and Thrombosis
Embolism and Thrombosis 		1 0 1 0.33 0 0
CUI: C0231618
Disease: Corkscrewing
Corkscrewing 		1 0 1 0.33 0 0
CUI: C0238408
Disease: Hematoma of rectus sheath
Hematoma of rectus sheath 		1 0 1 0.33 0 0
CUI: C0272328
Disease: Acquired factor X deficiency disease
Acquired factor X deficiency disease 		1 0 1 0.33 0 0
CUI: C0272355
Disease: von Willebrand disease, type IIC
von Willebrand disease, type IIC 		1 0 1 0.33 0 0
CUI: C0272356
Disease: von Willebrand disease, type IID
von Willebrand disease, type IID 		1 0 1 0.33 0 0
CUI: C0272363
Disease: ANTICOAGULANT DISORDERS
ANTICOAGULANT DISORDERS 		1 0 1 0.33 0 0
CUI: C0333183
Disease: Partial stenosis
Partial stenosis 		1 0 1 0.33 0 0
CUI: C0398610
Disease: Congenital von Willebrand's disease
Congenital von Willebrand's disease 		1 0 1 0.33 0 0
CUI: C0438921
Disease: Back Pain without Radiation
Back Pain without Radiation 		1 0 1 0.33 0 0
CUI: C0598480
Disease: intestinal angiodysplasia
intestinal angiodysplasia 		1 0 1 0.33 0 0
CUI: C0740363
Disease: Back Pain with Radiation
Back Pain with Radiation 		1 0 1 0.33 0 0
CUI: C0747194
Disease: Biliary acute pancreatitis
Biliary acute pancreatitis 		1 0 1 0.33 0 0
CUI: C0750949
Disease: Vertebrogenic Pain Syndrome
Vertebrogenic Pain Syndrome 		1 0 1 0.33 0 0
CUI: C0795843
Disease: Chromosome 12 ring
Chromosome 12 ring 		1 0 1 0.33 0 0
CUI: C0865262
Disease: Thrombopathy
Thrombopathy 		1 0 1 0.33 0 0
CUI: C0877172
Disease: Hematoma, Epidural, Spinal
Hematoma, Epidural, Spinal 		1 0 1 0.33 0 0
CUI: C0877456
Disease: Heyde's syndrome
Heyde's syndrome 		1 0 1 0.33 0 0
CUI: C1704212
Disease: Embolus
Embolus 		1 0 1 0.33 0 0
CUI: C1848525
Disease: von Willebrand Disease, Recessive Form
von Willebrand Disease, Recessive Form 		1 0 1 0.33 0 0
CUI: C2242682
Disease: Recurrent cerebral infarction
Recurrent cerebral infarction 		1 0 1 0.33 0 0
CUI: C2676721
Disease: Thrombophilia, Familial, Due To Decreased Release Of Tissue Plasminogen Activator
Thrombophilia, Familial, Due To Decreased Release Of Tissue Plasminogen Activator 		1 0 1 0.33 0 0