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: C1306557
Disease: Chronic venous insufficiency
Chronic venous insufficiency 		25 0 7 0.21 0 0
CUI: C2585317
Disease: Acquired thrombophilia
Acquired thrombophilia 		8 0 4 0.20 0 0
CUI: C0852077
Disease: Blood Coagulation Disorders, Inherited
Blood Coagulation Disorders, Inherited 		5 0 3 0.17 0 0
CUI: C0268615
Disease: 5,10-Methylenetetrahydrofolate reductase deficiency
5,10-Methylenetetrahydrofolate reductase deficiency 		6 0 3 0.16 0 0
CUI: C0338507
Disease: Non-arteritic ischemic optic neuropathy
Non-arteritic ischemic optic neuropathy 		6 0 3 0.16 0 0
CUI: C0584984
Disease: Heterozygous Factor V Leiden mutation
Heterozygous Factor V Leiden mutation 		6 0 3 0.16 0 0
CUI: C0000809
Disease: Abortion, Habitual
Abortion, Habitual 		7 0 3 0.15 0 0
CUI: C0007688
Disease: Central Retinal Artery Occlusion
Central Retinal Artery Occlusion 		7 0 3 0.15 0 0
CUI: C0035302
Disease: Retinal Artery Occlusion
Retinal Artery Occlusion 		9 0 3 0.14 0 0
CUI: C2721734
Disease: Methylenetetrahydrofolate reductase polymorphism
Methylenetetrahydrofolate reductase polymorphism 		9 0 3 0.14 0 0
CUI: C0242666
Disease: Protein S Deficiency
Protein S Deficiency 		19 0 4 0.13 0 0
CUI: C0749087
Disease: Thrombosis of subclavian vein
Thrombosis of subclavian vein 		2 0 2 0.12 0 0
CUI: C0751500
Disease: Petrous Sinus Thrombophlebitis
Petrous Sinus Thrombophlebitis 		2 0 2 0.12 0 0
CUI: C0751501
Disease: Intracranial Sinus Thrombophlebitis
Intracranial Sinus Thrombophlebitis 		2 0 2 0.12 0 0
CUI: C0751502
Disease: Petrous Sinus Thrombosis
Petrous Sinus Thrombosis 		2 0 2 0.12 0 0
CUI: C0752155
Disease: Central Nervous System Vascular Malformations
Central Nervous System Vascular Malformations 		2 0 2 0.12 0 0
CUI: C0919631
Disease: Upper Extremity Deep Vein Thrombosis, Primary
Upper Extremity Deep Vein Thrombosis, Primary 		2 0 2 0.12 0 0
CUI: C1610621
Disease: Factor II mutation
Factor II mutation 		2 0 2 0.12 0 0
CUI: C1856857
Disease: STROKE, ISCHEMIC, SUSCEPTIBILITY TO
STROKE, ISCHEMIC, SUSCEPTIBILITY TO 		2 0 2 0.12 0 0
CUI: C2584409
Disease: Prothrombin G20210A mutation
Prothrombin G20210A mutation 		20 0 4 0.12 0 0
CUI: C3805092
Disease: Methylenetetrahydrofolate reductase gene mutation
Methylenetetrahydrofolate reductase gene mutation 		11 0 3 0.12 0 0
CUI: C3852984
Disease: Acute Mesenteric Arterial Embolus
Acute Mesenteric Arterial Embolus 		2 0 2 0.12 0 0
CUI: C3852985
Disease: Occlusive Mesenteric Arterial Ischemia
Occlusive Mesenteric Arterial Ischemia 		2 0 2 0.12 0 0
CUI: C3852987
Disease: Acute Mesenteric Arterial Thrombosis
Acute Mesenteric Arterial Thrombosis 		2 0 2 0.12 0 0
CUI: C0013922
Disease: Embolism
Embolism 		3 0 2 0.12 0 0