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: C3888513
Disease: CYP2C9 polymorphism
CYP2C9 polymorphism 		3 0 3 0.30 0 0
CUI: C1709735
Disease: Prosthetic Valve Thrombosis
Prosthetic Valve Thrombosis 		8 0 4 0.29 0 0
CUI: C0020640
Disease: Inherited Factor II deficiency
Inherited Factor II deficiency 		2 0 2 0.20 0 0
CUI: C2675747
Disease: Coumarin Sensitivity
Coumarin Sensitivity 		2 0 2 0.20 0 0
CUI: C4280698
Disease: Reduced prothrombin antigen
Reduced prothrombin antigen 		2 0 2 0.20 0 0
CUI: C1867596
Disease: Hyperprothrombinemia
Hyperprothrombinemia 		4 0 2 0.17 0 0
CUI: C2363755
Disease: Acquired Protein S Deficiency
Acquired Protein S Deficiency 		4 0 2 0.17 0 0
CUI: C4024722
Disease: Reduced factor VII activity
Reduced factor VII activity 		4 0 2 0.17 0 0
CUI: C0042880
Disease: Vitamin K Deficiency
Vitamin K Deficiency 		19 0 4 0.16 0 0
CUI: C0032797
Disease: Postpartum Hemorrhage
Postpartum Hemorrhage 		6 0 2 0.14 0 0
CUI: C0240412
Disease: Muscle hematoma
Muscle hematoma 		6 0 2 0.14 0 0
CUI: C0584984
Disease: Heterozygous Factor V Leiden mutation
Heterozygous Factor V Leiden mutation 		6 0 2 0.14 0 0
CUI: C0750384
Disease: Coumarin Resistance
Coumarin Resistance 		6 0 2 0.14 0 0
CUI: C0019154
Disease: Hepatic Vein Thrombosis
Hepatic Vein Thrombosis 		23 0 4 0.14 0 0
CUI: C0268285
Disease: Adrenal hyperplasia, congenital, type 5
Adrenal hyperplasia, congenital, type 5 		7 0 2 0.13 0 0
CUI: C0856761
Disease: Budd-Chiari Syndrome
Budd-Chiari Syndrome 		24 0 4 0.13 0 0
CUI: C4321305
Disease: Consumptive Coagulopathy
Consumptive Coagulopathy 		9 0 2 0.12 0 0
CUI: C0015503
Disease: Factor VII Deficiency
Factor VII Deficiency 		10 0 2 0.11 0 0
CUI: C3669121
Disease: 11-Beta-hydroxylase deficiency
11-Beta-hydroxylase deficiency 		10 0 2 0.11 0 0
CUI: C0268292
Disease: Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency
Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency 		11 0 2 0.11 0 0
CUI: C0152097
Disease: Disease of diaphragm
Disease of diaphragm 		1 0 1 1.0E-01 0 0
CUI: C0266785
Disease: Abnormal umbilical cord
Abnormal umbilical cord 		1 0 1 1.0E-01 0 0
CUI: C0267406
Disease: Mesenteric infarction
Mesenteric infarction 		1 0 1 1.0E-01 0 0
CUI: C0494290
Disease: Type 2 diabetes mellitus without complication
Type 2 diabetes mellitus without complication 		1 0 1 1.0E-01 0 0
CUI: C0584983
Disease: Homozygous Factor V Leiden mutation
Homozygous Factor V Leiden mutation 		1 0 1 1.0E-01 0 0