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: C0040015
Disease: Thrombasthenia
Thrombasthenia 		48 0 14 0.11 0 0
CUI: C2584620
Disease: Thrombophilia, hereditary
Thrombophilia, hereditary 		17 0 11 0.11 0 0
CUI: C0751956
Disease: Acute Cerebrovascular Accidents
Acute Cerebrovascular Accidents 		155 0 24 0.10 0 0
CUI: C0042974
Disease: von Willebrand Disease
von Willebrand Disease 		62 0 15 0.10 0 0
CUI: C0007820
Disease: Cerebrovascular Disorders
Cerebrovascular Disorders 		233 0 31 0.10 0 0
CUI: C0013491
Disease: Ecchymosis
Ecchymosis 		41 0 13 0.10 0 0
CUI: C0272285
Disease: Heparin-induced thrombocytopenia
Heparin-induced thrombocytopenia 		44 0 13 0.10 0 0
CUI: C0025323
Disease: Menorrhagia
Menorrhagia 		34 0 12 1.0E-01 0 0
CUI: C0151945
Disease: Thrombosis of cerebral veins
Thrombosis of cerebral veins 		35 0 12 9.9E-02 0 0
CUI: C0856761
Disease: Budd-Chiari Syndrome
Budd-Chiari Syndrome 		24 0 11 9.9E-02 0 0
CUI: C0007273
Disease: Carotid Artery Diseases
Carotid Artery Diseases 		69 0 15 9.9E-02 0 0
CUI: C0577631
Disease: Carotid Atherosclerosis
Carotid Atherosclerosis 		219 0 28 9.7E-02 0 0
CUI: C0032914
Disease: Pre-Eclampsia
Pre-Eclampsia 		166 0 23 9.5E-02 0 0
CUI: C0035328
Disease: Retinal Vein Occlusion
Retinal Vein Occlusion 		76 0 15 9.4E-02 0 0
CUI: C0019087
Disease: Hemorrhagic Disorders
Hemorrhagic Disorders 		30 0 11 9.4E-02 0 0
CUI: C0242666
Disease: Protein S Deficiency
Protein S Deficiency 		19 0 10 9.3E-02 0 0
CUI: C2584409
Disease: Prothrombin G20210A mutation
Prothrombin G20210A mutation 		20 0 10 9.3E-02 0 0
CUI: C0085096
Disease: Peripheral Vascular Diseases
Peripheral Vascular Diseases 		150 0 21 9.3E-02 0 0
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome 		440 0 45 9.1E-02 0 0
CUI: C0085409
Disease: Polyendocrinopathies, Autoimmune
Polyendocrinopathies, Autoimmune 		166 0 22 9.1E-02 0 0
CUI: C0019154
Disease: Hepatic Vein Thrombosis
Hepatic Vein Thrombosis 		23 0 10 9.0E-02 0 0
CUI: C1260403
Disease: prothrombin gene mutation
prothrombin gene mutation 		23 0 10 9.0E-02 0 0
CUI: C0235574
Disease: Intravascular hemolysis
Intravascular hemolysis 		36 0 11 8.9E-02 0 0
CUI: C2937358
Disease: Cerebral Hemorrhage
Cerebral Hemorrhage 		122 0 18 8.9E-02 0 0
CUI: C0007282
Disease: Carotid Stenosis
Carotid Stenosis 		135 0 19 8.9E-02 0 0