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: C0087086
Disease: Thrombus
Thrombus 		46 0 14 0.22 0 0
CUI: C0034065
Disease: Pulmonary Embolism
Pulmonary Embolism 		93 16 18 0.17 1 4.8E-02
CUI: C3805092
Disease: Methylenetetrahydrofolate reductase gene mutation
Methylenetetrahydrofolate reductase gene mutation 		11 3 6 0.16 2 0.29
CUI: C0600433
Disease: Activated Protein C Resistance
Activated Protein C Resistance 		41 30 10 0.16 4 0.12
CUI: C0040053
Disease: Thrombosis
Thrombosis 		98 0 17 0.15 0 0
CUI: C1260403
Disease: prothrombin gene mutation
prothrombin gene mutation 		23 5 7 0.14 3 0.38
CUI: C0040038
Disease: Thromboembolism
Thromboembolism 		25 0 7 0.14 0 0
CUI: C1273976
Disease: First myocardial infarction
First myocardial infarction 		17 0 6 0.14 0 0
CUI: C2584620
Disease: Thrombophilia, hereditary
Thrombophilia, hereditary 		17 9 6 0.14 3 0.25
CUI: C0242666
Disease: Protein S Deficiency
Protein S Deficiency 		19 14 6 0.13 4 0.25
CUI: C0032320
Disease: Pneumoperitoneum
Pneumoperitoneum 		28 0 7 0.13 0 0
CUI: C1096458
Disease: Vascular occlusion
Vascular occlusion 		30 2 7 0.12 2 0.33
CUI: C3805089
Disease: Hyperfibrinolysis
Hyperfibrinolysis 		12 0 5 0.12 0 0
CUI: C1260903
Disease: Dysfibrinogenemia
Dysfibrinogenemia 		13 6 5 0.12 1 9.1E-02
CUI: C0019154
Disease: Hepatic Vein Thrombosis
Hepatic Vein Thrombosis 		23 4 6 0.12 2 0.25
CUI: C0398625
Disease: Protein C Deficiency
Protein C Deficiency 		43 14 8 0.12 3 0.18
CUI: C0856761
Disease: Budd-Chiari Syndrome
Budd-Chiari Syndrome 		24 4 6 0.12 2 0.25
CUI: C0079102
Disease: Cerebral Thrombosis
Cerebral Thrombosis 		15 7 5 0.12 3 0.30
CUI: C0162529
Disease: Colitis, Ischemic
Colitis, Ischemic 		15 3 5 0.12 1 0.12
CUI: C0026766
Disease: Multiple Organ Failure
Multiple Organ Failure 		25 0 6 0.12 0 0
CUI: C0151945
Disease: Thrombosis of cerebral veins
Thrombosis of cerebral veins 		35 11 7 0.11 3 0.21
CUI: C0584984
Disease: Heterozygous Factor V Leiden mutation
Heterozygous Factor V Leiden mutation 		6 0 4 0.11 0 0
CUI: C2609046
Disease: Sticky platelet syndrome
Sticky platelet syndrome 		6 2 4 0.11 1 0.14
CUI: C0015499
Disease: Hereditary Factor V Deficiency
Hereditary Factor V Deficiency 		7 7 4 0.11 1 8.3E-02
CUI: C0037198
Disease: Sinus Thrombosis, Intracranial
Sinus Thrombosis, Intracranial 		17 5 5 0.11 2 0.22