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: C0584960
Disease: Factor V Leiden mutation
Factor V Leiden mutation 		86 46 47 0.25 19 0.27
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis 		217 76 69 0.23 18 0.18
CUI: C0311370
Disease: Lupus anticoagulant disorder
Lupus anticoagulant disorder 		61 14 36 0.21 7 0.14
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		270 106 71 0.20 21 0.16
CUI: C0012739
Disease: Disseminated Intravascular Coagulation
Disseminated Intravascular Coagulation 		94 0 40 0.20 0 0
CUI: C0085278
Disease: Antiphospholipid Syndrome
Antiphospholipid Syndrome 		89 11 39 0.20 4 8.0E-02
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders 		233 27 57 0.18 5 7.7E-02
CUI: C0600433
Disease: Activated Protein C Resistance
Activated Protein C Resistance 		40 23 28 0.17 15 0.29
CUI: C0085409
Disease: Polyendocrinopathies, Autoimmune
Polyendocrinopathies, Autoimmune 		163 0 44 0.16 0 0
CUI: C0019069
Disease: Hemophilia A
Hemophilia A 		142 36 40 0.16 5 6.8E-02
CUI: C0398625
Disease: Protein C Deficiency
Protein C Deficiency 		41 8 26 0.16 4 8.5E-02
CUI: C1963943
Disease: Atherothrombosis
Atherothrombosis 		115 15 34 0.15 5 9.4E-02
CUI: C0155773
Disease: Portal Vein Thrombosis
Portal Vein Thrombosis 		56 8 26 0.15 5 0.11
CUI: C2717961
Disease: Thrombotic Microangiopathies
Thrombotic Microangiopathies 		60 8 24 0.13 3 6.2E-02
CUI: C0085096
Disease: Peripheral Vascular Diseases
Peripheral Vascular Diseases 		144 17 33 0.13 5 9.1E-02
CUI: C0751956
Disease: Acute Cerebrovascular Accidents
Acute Cerebrovascular Accidents 		111 0 29 0.13 0 0
CUI: C0007820
Disease: Cerebrovascular Disorders
Cerebrovascular Disorders 		231 56 42 0.12 4 4.2E-02
CUI: C0040034
Disease: Thrombocytopenia
Thrombocytopenia 		376 69 57 0.12 3 2.8E-02
CUI: C0035328
Disease: Retinal Vein Occlusion
Retinal Vein Occlusion 		64 15 23 0.12 9 0.18
CUI: C0272322
Disease: Severe hereditary factor VIII deficiency disease
Severe hereditary factor VIII deficiency disease 		37 15 20 0.12 6 0.12
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases 		279 54 46 0.12 9 0.10
CUI: C1719672
Disease: Severe Sepsis
Severe Sepsis 		168 29 34 0.12 1 1.4E-02
CUI: C0598608
Disease: Hyperhomocysteinemia
Hyperhomocysteinemia 		225 45 40 0.12 12 0.16
CUI: C0151945
Disease: Thrombosis of cerebral veins
Thrombosis of cerebral veins 		31 11 19 0.12 6 0.12
CUI: C1260403
Disease: prothrombin gene mutation
prothrombin gene mutation 		23 5 18 0.12 5 0.12