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: C0866188
Disease: Renal thrombosis
Renal thrombosis 		1 0 1 1.00 0 0
CUI: C2585960
Disease: Heterozygous protein C deficiency
Heterozygous protein C deficiency 		1 0 1 1.00 0 0
CUI: C2674321
Disease: Thrombophilia, Hereditary, Due To Protein C Deficiency, Autosomal Dominant
Thrombophilia, Hereditary, Due To Protein C Deficiency, Autosomal Dominant 		1 41 1 1.00 5 0.10
CUI: C2674322
Disease: Protein C Deficiency, Acquired
Protein C Deficiency, Acquired 		1 0 1 1.00 0 0
CUI: C4329969
Disease: Factor VIII Inactivation
Factor VIII Inactivation 		1 0 1 1.00 0 0
CUI: C4708643
Disease: Acroangiodermatitis of skin
Acroangiodermatitis of skin 		1 0 1 1.00 0 0
CUI: C0339499
Disease: Central retinal vein occlusion - juvenile
Central retinal vein occlusion - juvenile 		2 0 1 0.50 0 0
CUI: C0341426
Disease: Small intestinal infarction
Small intestinal infarction 		2 0 1 0.50 0 0
CUI: C1861171
Disease: THROMBOPHILIA DUE TO ACTIVATED PROTEIN C RESISTANCE (disorder)
THROMBOPHILIA DUE TO ACTIVATED PROTEIN C RESISTANCE (disorder) 		2 0 1 0.50 0 0
CUI: C1867638
Disease: Warfarin-induced skin necrosis
Warfarin-induced skin necrosis 		2 0 1 0.50 0 0
CUI: C2930896
Disease: Congenital thrombotic disease, due to Protein C deficiency
Congenital thrombotic disease, due to Protein C deficiency 		2 0 1 0.50 0 0
CUI: C1856143
Disease: HEMOLYTIC UREMIC SYNDROME, TYPICAL
HEMOLYTIC UREMIC SYNDROME, TYPICAL 		3 0 1 0.33 0 0
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		3 0 1 0.33 0 0
CUI: C4553919
Disease: Superficial Thrombophlebitis, CTCAE
Superficial Thrombophlebitis, CTCAE 		3 0 1 0.33 0 0
CUI: C1867596
Disease: Hyperprothrombinemia
Hyperprothrombinemia 		4 0 1 0.25 0 0
CUI: C2363755
Disease: Acquired Protein S Deficiency
Acquired Protein S Deficiency 		4 0 1 0.25 0 0
CUI: C0003860
Disease: Arteritis
Arteritis 		5 0 1 0.20 0 0
CUI: C1510431
Disease: Superficial Thrombophlebitis
Superficial Thrombophlebitis 		5 0 1 0.20 0 0
CUI: C3164780
Disease: Clinical sepsis
Clinical sepsis 		5 0 1 0.20 0 0
CUI: C0584984
Disease: Heterozygous Factor V Leiden mutation
Heterozygous Factor V Leiden mutation 		6 0 1 0.17 0 0
CUI: C1299567
Disease: Neonatal stroke
Neonatal stroke 		8 0 1 0.12 0 0
CUI: C4321305
Disease: Consumptive Coagulopathy
Consumptive Coagulopathy 		9 0 1 0.11 0 0
CUI: C2608079
Disease: WARFARIN SENSITIVITY (disorder)
WARFARIN SENSITIVITY (disorder) 		10 0 1 1.0E-01 0 0
CUI: C3536663
Disease: Acute deep venous thrombosis
Acute deep venous thrombosis 		11 0 1 9.1E-02 0 0
CUI: C0042909
Disease: Vitreous Hemorrhage
Vitreous Hemorrhage 		12 0 1 8.3E-02 0 0