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: C0584960
Disease: Factor V Leiden mutation
Factor V Leiden mutation 		86 46 46 0.17 21 0.18
CUI: C0398623
Disease: Thrombophilia
Thrombophilia 		161 43 72 0.23 19 0.16
CUI: C0034065
Disease: Pulmonary Embolism
Pulmonary Embolism 		93 16 39 0.14 12 0.12
CUI: C0598608
Disease: Hyperhomocysteinemia
Hyperhomocysteinemia 		246 45 56 0.13 15 0.12
CUI: C0035328
Disease: Retinal Vein Occlusion
Retinal Vein Occlusion 		76 15 31 0.11 10 0.10
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		378 408 97 0.19 45 9.9E-02
CUI: C0600433
Disease: Activated Protein C Resistance
Activated Protein C Resistance 		41 30 29 0.12 11 9.8E-02
CUI: C4552766
Disease: Miscarriage
Miscarriage 		426 56 53 8.8E-02 12 8.8E-02
CUI: C0240912
Disease: Vertical Talus
Vertical Talus 		69 20 11 3.8E-02 9 8.7E-02
CUI: C0035344
Disease: Retinopathy of Prematurity
Retinopathy of Prematurity 		202 16 30 7.5E-02 8 7.9E-02
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation 		1037 21 69 5.8E-02 8 7.5E-02
CUI: C0151945
Disease: Thrombosis of cerebral veins
Thrombosis of cerebral veins 		35 11 20 8.2E-02 7 7.2E-02
CUI: C0242666
Disease: Protein S Deficiency
Protein S Deficiency 		19 14 13 5.5E-02 7 7.0E-02
CUI: C0272375
Disease: Antithrombin III Deficiency
Antithrombin III Deficiency 		27 52 13 5.3E-02 9 6.6E-02
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction 		766 118 105 0.12 13 6.6E-02
CUI: C2584409
Disease: Prothrombin G20210A mutation
Prothrombin G20210A mutation 		20 9 13 5.5E-02 6 6.2E-02
CUI: C2584620
Disease: Thrombophilia, hereditary
Thrombophilia, hereditary 		17 9 15 6.5E-02 6 6.2E-02
CUI: C0042847
Disease: Vitamin B 12 Deficiency
Vitamin B 12 Deficiency 		29 11 4 1.6E-02 6 6.1E-02
CUI: C0398625
Disease: Protein C Deficiency
Protein C Deficiency 		43 14 22 8.8E-02 6 5.9E-02
CUI: C0272322
Disease: Severe hereditary factor VIII deficiency disease
Severe hereditary factor VIII deficiency disease 		37 15 15 6.0E-02 6 5.9E-02
CUI: C0025281
Disease: Meniere Disease
Meniere Disease 		69 36 13 4.5E-02 7 5.7E-02
CUI: C0085096
Disease: Peripheral Vascular Diseases
Peripheral Vascular Diseases 		150 18 42 0.12 6 5.7E-02
CUI: C0013537
Disease: Eclampsia
Eclampsia 		241 38 45 0.11 7 5.6E-02
CUI: C4275242
Disease: Sudden sensorineural hearing loss
Sudden sensorineural hearing loss 		72 38 18 6.3E-02 7 5.6E-02
CUI: C0042373
Disease: Vascular Diseases
Vascular Diseases 		688 40 97 0.12 7 5.6E-02