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: C0339505
Disease: Venous retinal branch occlusion
Venous retinal branch occlusion 		25 7 14 0.29 6 0.75
CUI: C1260403
Disease: prothrombin gene mutation
prothrombin gene mutation 		23 5 10 0.20 3 0.33
CUI: C0242666
Disease: Protein S Deficiency
Protein S Deficiency 		19 14 9 0.19 3 0.17
CUI: C0035328
Disease: Retinal Vein Occlusion
Retinal Vein Occlusion 		76 15 16 0.16 3 0.16
CUI: C0007688
Disease: Central Retinal Artery Occlusion
Central Retinal Artery Occlusion 		7 0 6 0.15 0 0
CUI: C0079102
Disease: Cerebral Thrombosis
Cerebral Thrombosis 		15 7 7 0.15 2 0.17
CUI: C0398621
Disease: Hypoplasminogenemia
Hypoplasminogenemia 		9 3 6 0.15 1 0.11
CUI: C0795687
Disease: Cerebral arterial thrombosis
Cerebral arterial thrombosis 		14 9 6 0.13 2 0.14
CUI: C0162529
Disease: Colitis, Ischemic
Colitis, Ischemic 		15 3 6 0.13 1 0.11
CUI: C0584960
Disease: Factor V Leiden mutation
Factor V Leiden mutation 		86 46 14 0.13 3 6.0E-02
CUI: C3665926
Disease: Myopic choroidal neovascularization
Myopic choroidal neovascularization 		7 0 5 0.12 0 0
CUI: C0010072
Disease: Coronary Thrombosis
Coronary Thrombosis 		35 0 8 0.12 0 0
CUI: C0151945
Disease: Thrombosis of cerebral veins
Thrombosis of cerebral veins 		35 11 8 0.12 2 0.12
CUI: C0338573
Disease: Cerebral venous sinus thrombosis
Cerebral venous sinus thrombosis 		17 1 6 0.12 1 0.14
CUI: C2584620
Disease: Thrombophilia, hereditary
Thrombophilia, hereditary 		17 9 6 0.12 3 0.23
CUI: C2585317
Disease: Acquired thrombophilia
Acquired thrombophilia 		8 2 5 0.12 1 0.12
CUI: C0035302
Disease: Retinal Artery Occlusion
Retinal Artery Occlusion 		9 1 5 0.12 1 0.14
CUI: C2584409
Disease: Prothrombin G20210A mutation
Prothrombin G20210A mutation 		20 9 6 0.12 3 0.23
CUI: C0155773
Disease: Portal Vein Thrombosis
Portal Vein Thrombosis 		59 8 10 0.11 3 0.25
CUI: C3805092
Disease: Methylenetetrahydrofolate reductase gene mutation
Methylenetetrahydrofolate reductase gene mutation 		11 3 5 0.11 1 0.11
CUI: C3495426
Disease: Homocysteinemia
Homocysteinemia 		21 6 6 0.11 2 0.18
CUI: C0600433
Disease: Activated Protein C Resistance
Activated Protein C Resistance 		41 30 8 0.11 3 8.8E-02
CUI: C1852242
Disease: Nonarteritic anterior ischemic optic neuropathy (NAION)
Nonarteritic anterior ischemic optic neuropathy (NAION) 		22 6 6 0.11 3 0.30
CUI: C0398625
Disease: Protein C Deficiency
Protein C Deficiency 		43 14 8 0.11 2 0.11
CUI: C0019154
Disease: Hepatic Vein Thrombosis
Hepatic Vein Thrombosis 		23 4 6 0.11 2 0.22