Source: BEFREE ×
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: C0079102
Disease: Cerebral Thrombosis
Cerebral Thrombosis 		13 7 13 0.42 7 0.64
CUI: C0795687
Disease: Cerebral arterial thrombosis
Cerebral arterial thrombosis 		14 9 13 0.41 7 0.54
CUI: C2584620
Disease: Thrombophilia, hereditary
Thrombophilia, hereditary 		17 9 11 0.30 5 0.33
CUI: C0242666
Disease: Protein S Deficiency
Protein S Deficiency 		19 14 11 0.28 3 0.14
CUI: C1260403
Disease: prothrombin gene mutation
prothrombin gene mutation 		23 5 11 0.26 4 0.33
CUI: C0338573
Disease: Cerebral venous sinus thrombosis
Cerebral venous sinus thrombosis 		17 1 9 0.23 1 9.1E-02
CUI: C0272375
Disease: Antithrombin III Deficiency
Antithrombin III Deficiency 		19 9 9 0.22 3 0.18
CUI: C2585317
Disease: Acquired thrombophilia
Acquired thrombophilia 		8 2 7 0.22 2 0.18
CUI: C0240912
Disease: Vertical Talus
Vertical Talus 		29 15 10 0.20 7 0.37
CUI: C3805092
Disease: Methylenetetrahydrofolate reductase gene mutation
Methylenetetrahydrofolate reductase gene mutation 		11 3 7 0.20 2 0.17
CUI: C2584409
Disease: Prothrombin G20210A mutation
Prothrombin G20210A mutation 		20 9 8 0.19 4 0.25
CUI: C0600433
Disease: Activated Protein C Resistance
Activated Protein C Resistance 		40 23 11 0.18 6 0.21
CUI: C0019154
Disease: Hepatic Vein Thrombosis
Hepatic Vein Thrombosis 		21 4 8 0.18 3 0.25
CUI: C3495426
Disease: Homocysteinemia
Homocysteinemia 		21 6 8 0.18 5 0.42
CUI: C0856761
Disease: Budd-Chiari Syndrome
Budd-Chiari Syndrome 		22 4 8 0.18 3 0.25
CUI: C0398621
Disease: Hypoplasminogenemia
Hypoplasminogenemia 		9 3 6 0.18 2 0.17
CUI: C0311370
Disease: Lupus anticoagulant disorder
Lupus anticoagulant disorder 		61 14 13 0.16 4 0.19
CUI: C0398625
Disease: Protein C Deficiency
Protein C Deficiency 		41 8 10 0.16 3 0.19
CUI: C0155773
Disease: Portal Vein Thrombosis
Portal Vein Thrombosis 		56 8 12 0.16 4 0.27
CUI: C0584960
Disease: Factor V Leiden mutation
Factor V Leiden mutation 		86 46 16 0.16 7 0.14
CUI: C0584984
Disease: Heterozygous Factor V Leiden mutation
Heterozygous Factor V Leiden mutation 		6 0 5 0.16 0 0
CUI: C0034341
Disease: Pyruvate Carboxylase Deficiency Disease
Pyruvate Carboxylase Deficiency Disease 		14 0 6 0.15 0 0
CUI: C0039240
Disease: Supraventricular tachycardia
Supraventricular tachycardia 		22 6 7 0.15 2 0.13
CUI: C0007688
Disease: Central Retinal Artery Occlusion
Central Retinal Artery Occlusion 		7 0 5 0.15 0 0
CUI: C0162529
Disease: Colitis, Ischemic
Colitis, Ischemic 		15 3 6 0.15 3 0.27