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: C0242666
Disease: Protein S Deficiency
Protein S Deficiency 		19 14 8 0.29 1 7.1E-02
CUI: C0007688
Disease: Central Retinal Artery Occlusion
Central Retinal Artery Occlusion 		7 0 5 0.26 0 0
CUI: C2584620
Disease: Thrombophilia, hereditary
Thrombophilia, hereditary 		17 9 7 0.26 1 0.11
CUI: C1260403
Disease: prothrombin gene mutation
prothrombin gene mutation 		23 5 7 0.21 1 0.20
CUI: C0584984
Disease: Heterozygous Factor V Leiden mutation
Heterozygous Factor V Leiden mutation 		6 0 4 0.21 0 0
CUI: C0151945
Disease: Thrombosis of cerebral veins
Thrombosis of cerebral veins 		35 11 9 0.21 1 9.1E-02
CUI: C0040038
Disease: Thromboembolism
Thromboembolism 		25 0 7 0.20 0 0
CUI: C0795687
Disease: Cerebral arterial thrombosis
Cerebral arterial thrombosis 		14 9 5 0.19 1 0.11
CUI: C2585317
Disease: Acquired thrombophilia
Acquired thrombophilia 		8 2 4 0.19 1 0.50
CUI: C3495426
Disease: Homocysteinemia
Homocysteinemia 		21 6 6 0.19 1 0.17
CUI: C0079102
Disease: Cerebral Thrombosis
Cerebral Thrombosis 		15 7 5 0.19 1 0.14
CUI: C0398621
Disease: Hypoplasminogenemia
Hypoplasminogenemia 		9 3 4 0.18 1 0.33
CUI: C0267412
Disease: Mesenteric Venous Thrombosis
Mesenteric Venous Thrombosis 		3 0 3 0.18 0 0
CUI: C0745497
Disease: Thrombosis of internal jugular vein
Thrombosis of internal jugular vein 		3 0 3 0.18 0 0
CUI: C3665816
Disease: Perinatal stroke
Perinatal stroke 		3 0 3 0.18 0 0
CUI: C0037198
Disease: Sinus Thrombosis, Intracranial
Sinus Thrombosis, Intracranial 		17 5 5 0.17 1 0.20
CUI: C0238457
Disease: Thrombosis of renal vein
Thrombosis of renal vein 		4 0 3 0.17 0 0
CUI: C2363755
Disease: Acquired Protein S Deficiency
Acquired Protein S Deficiency 		4 0 3 0.17 0 0
CUI: C3805092
Disease: Methylenetetrahydrofolate reductase gene mutation
Methylenetetrahydrofolate reductase gene mutation 		11 3 4 0.17 1 0.33
CUI: C0600433
Disease: Activated Protein C Resistance
Activated Protein C Resistance 		41 30 8 0.16 1 3.3E-02
CUI: C0238096
Disease: Embolism, Paradoxical
Embolism, Paradoxical 		5 0 3 0.16 0 0
CUI: C0272375
Disease: Antithrombin III Deficiency
Antithrombin III Deficiency 		27 52 6 0.16 1 1.9E-02
CUI: C0338575
Disease: Sagittal Sinus Thrombosis
Sagittal Sinus Thrombosis 		5 0 3 0.16 0 0
CUI: C0852077
Disease: Blood Coagulation Disorders, Inherited
Blood Coagulation Disorders, Inherited 		5 0 3 0.16 0 0
CUI: C1510431
Disease: Superficial Thrombophlebitis
Superficial Thrombophlebitis 		5 0 3 0.16 0 0