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: C0600433
Disease: Activated Protein C Resistance
Activated Protein C Resistance 		41 30 28 0.28 18 0.31
CUI: C0398625
Disease: Protein C Deficiency
Protein C Deficiency 		43 14 26 0.25 4 7.1E-02
CUI: C0398623
Disease: Thrombophilia
Thrombophilia 		161 43 47 0.23 19 0.27
CUI: C0311370
Disease: Lupus anticoagulant disorder
Lupus anticoagulant disorder 		66 14 28 0.23 6 0.11
CUI: C1260403
Disease: prothrombin gene mutation
prothrombin gene mutation 		23 5 20 0.22 5 0.11
CUI: C0040053
Disease: Thrombosis
Thrombosis 		98 0 30 0.19 0 0
CUI: C0151945
Disease: Thrombosis of cerebral veins
Thrombosis of cerebral veins 		35 11 18 0.17 7 0.14
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis 		230 93 46 0.17 21 0.18
CUI: C0012739
Disease: Disseminated Intravascular Coagulation
Disseminated Intravascular Coagulation 		117 0 29 0.17 0 0
CUI: C0242666
Disease: Protein S Deficiency
Protein S Deficiency 		19 14 15 0.17 8 0.15
CUI: C2584620
Disease: Thrombophilia, hereditary
Thrombophilia, hereditary 		17 9 14 0.16 7 0.15
CUI: C0272375
Disease: Antithrombin III Deficiency
Antithrombin III Deficiency 		27 52 15 0.15 6 6.5E-02
CUI: C2584409
Disease: Prothrombin G20210A mutation
Prothrombin G20210A mutation 		20 9 14 0.15 7 0.15
CUI: C0155773
Disease: Portal Vein Thrombosis
Portal Vein Thrombosis 		59 8 19 0.15 6 0.12
CUI: C0035328
Disease: Retinal Vein Occlusion
Retinal Vein Occlusion 		76 15 21 0.15 10 0.20
CUI: C0085278
Disease: Antiphospholipid Syndrome
Antiphospholipid Syndrome 		99 17 23 0.14 3 5.0E-02
CUI: C0010072
Disease: Coronary Thrombosis
Coronary Thrombosis 		35 2 15 0.14 1 2.1E-02
CUI: C2717961
Disease: Thrombotic Microangiopathies
Thrombotic Microangiopathies 		62 8 18 0.14 3 5.9E-02
CUI: C0019880
Disease: Homocystinuria
Homocystinuria 		39 0 15 0.14 0 0
CUI: C1963943
Disease: Atherothrombosis
Atherothrombosis 		115 15 24 0.14 3 5.2E-02
CUI: C0272322
Disease: Severe hereditary factor VIII deficiency disease
Severe hereditary factor VIII deficiency disease 		37 15 14 0.13 6 0.11
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		117 218 23 0.13 2 7.6E-03
CUI: C0684275
Disease: Hemophilia, NOS
Hemophilia, NOS 		82 8 19 0.13 1 1.9E-02
CUI: C0154841
Disease: Central retinal vein occlusion
Central retinal vein occlusion 		38 7 14 0.13 3 6.0E-02
CUI: C0852949
Disease: Arteriopathic disease
Arteriopathic disease 		101 14 21 0.13 2 3.4E-02