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: C0749087
Disease: Thrombosis of subclavian vein
Thrombosis of subclavian vein 		2 0 2 0.33 0 0
CUI: C0752155
Disease: Central Nervous System Vascular Malformations
Central Nervous System Vascular Malformations 		2 0 2 0.33 0 0
CUI: C0919631
Disease: Upper Extremity Deep Vein Thrombosis, Primary
Upper Extremity Deep Vein Thrombosis, Primary 		2 0 2 0.33 0 0
CUI: C1856857
Disease: STROKE, ISCHEMIC, SUSCEPTIBILITY TO
STROKE, ISCHEMIC, SUSCEPTIBILITY TO 		2 0 2 0.33 0 0
CUI: C3852984
Disease: Acute Mesenteric Arterial Embolus
Acute Mesenteric Arterial Embolus 		2 0 2 0.33 0 0
CUI: C3852985
Disease: Occlusive Mesenteric Arterial Ischemia
Occlusive Mesenteric Arterial Ischemia 		2 0 2 0.33 0 0
CUI: C3852987
Disease: Acute Mesenteric Arterial Thrombosis
Acute Mesenteric Arterial Thrombosis 		2 0 2 0.33 0 0
CUI: C0013922
Disease: Embolism
Embolism 		3 0 2 0.29 0 0
CUI: C0267412
Disease: Mesenteric Venous Thrombosis
Mesenteric Venous Thrombosis 		3 0 2 0.29 0 0
CUI: C0745497
Disease: Thrombosis of internal jugular vein
Thrombosis of internal jugular vein 		3 0 2 0.29 0 0
CUI: C2585350
Disease: Hereditary hyperhomocysteinemia
Hereditary hyperhomocysteinemia 		3 0 2 0.29 0 0
CUI: C3852986
Disease: Nonocclusive Mesenteric Ischemia
Nonocclusive Mesenteric Ischemia 		3 0 2 0.29 0 0
CUI: C0032807
Disease: Postphlebitic Syndrome
Postphlebitic Syndrome 		4 0 2 0.25 0 0
CUI: C0238096
Disease: Embolism, Paradoxical
Embolism, Paradoxical 		5 0 2 0.22 0 0
CUI: C0852077
Disease: Blood Coagulation Disorders, Inherited
Blood Coagulation Disorders, Inherited 		5 0 2 0.22 0 0
CUI: C3805092
Disease: Methylenetetrahydrofolate reductase gene mutation
Methylenetetrahydrofolate reductase gene mutation 		11 3 3 0.21 1 0.25
CUI: C0085642
Disease: Livedo Reticularis
Livedo Reticularis 		6 0 2 0.20 0 0
CUI: C0268615
Disease: 5,10-Methylenetetrahydrofolate reductase deficiency
5,10-Methylenetetrahydrofolate reductase deficiency 		6 0 2 0.20 0 0
CUI: C0272350
Disease: Dysfibrinogenemia, Congenital
Dysfibrinogenemia, Congenital 		6 0 2 0.20 0 0
CUI: C0338507
Disease: Non-arteritic ischemic optic neuropathy
Non-arteritic ischemic optic neuropathy 		6 0 2 0.20 0 0
CUI: C0584984
Disease: Heterozygous Factor V Leiden mutation
Heterozygous Factor V Leiden mutation 		6 0 2 0.20 0 0
CUI: C4317320
Disease: Factor V deficiency
Factor V deficiency 		6 0 2 0.20 0 0
CUI: C1260903
Disease: Dysfibrinogenemia
Dysfibrinogenemia 		13 0 3 0.19 0 0
CUI: C0000809
Disease: Abortion, Habitual
Abortion, Habitual 		7 0 2 0.18 0 0
CUI: C0015499
Disease: Hereditary Factor V Deficiency
Hereditary Factor V Deficiency 		7 0 2 0.18 0 0