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: C3494187
Disease: Factor VIII Deficiency
Factor VIII Deficiency 		9 0 3 0.30 0 0
CUI: C0521533
Disease: Atrial septal aneurysm
Atrial septal aneurysm 		5 0 2 0.29 0 0
CUI: C0852077
Disease: Blood Coagulation Disorders, Inherited
Blood Coagulation Disorders, Inherited 		5 0 2 0.29 0 0
CUI: C0270805
Disease: Hemiplegic cerebral palsy
Hemiplegic cerebral palsy 		1 0 1 0.25 0 0
CUI: C0272275
Disease: Heparin-induced thrombocytopenia with thrombosis
Heparin-induced thrombocytopenia with thrombosis 		1 0 1 0.25 0 0
CUI: C0272328
Disease: Acquired factor X deficiency disease
Acquired factor X deficiency disease 		1 0 1 0.25 0 0
CUI: C0272334
Disease: Hereditary factor XII deficiency disease
Hereditary factor XII 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: C0343081
Disease: Livedoid vasculitis
Livedoid vasculitis 		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: C0589110
Disease: Postoperative deep vein thrombosis
Postoperative deep vein thrombosis 		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: C0854142
Disease: Thrombosis of aorta
Thrombosis of aorta 		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: C1096488
Disease: Hereditary factor IX deficiency disease without inhibitor
Hereditary factor IX deficiency disease without inhibitor 		1 0 1 0.25 0 0
CUI: C1397674
Disease: Persistent foramen ovale
Persistent foramen ovale 		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: C1853831
Disease: Bleeding Disorder, East Texas Type
Bleeding Disorder, East Texas Type 		1 0 1 0.25 0 0
CUI: C1960459
Disease: Hereditary angioedema with normal C1 esterase inhibitor activity
Hereditary angioedema with normal C1 esterase inhibitor activity 		1 0 1 0.25 0 0
CUI: C2676744
Disease: BUDD-CHIARI SYNDROME, SUSCEPTIBILITY TO
BUDD-CHIARI SYNDROME, SUSCEPTIBILITY TO 		1 0 1 0.25 0 0
CUI: C2749016
Disease: Thrombophilia, X-Linked, Due To Factor Ix Defect
Thrombophilia, X-Linked, Due To Factor Ix Defect 		1 0 1 0.25 0 0