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: C2584620
Disease: Thrombophilia, hereditary
Thrombophilia, hereditary 		17 0 7 0.26 0 0
CUI: C0079102
Disease: Cerebral Thrombosis
Cerebral Thrombosis 		15 0 6 0.23 0 0
CUI: C3272265
Disease: Three Vessel Coronary Disease
Three Vessel Coronary Disease 		11 0 5 0.22 0 0
CUI: C0268615
Disease: 5,10-Methylenetetrahydrofolate reductase deficiency
5,10-Methylenetetrahydrofolate reductase deficiency 		6 0 4 0.21 0 0
CUI: C0035302
Disease: Retinal Artery Occlusion
Retinal Artery Occlusion 		9 0 4 0.18 0 0
CUI: C0013922
Disease: Embolism
Embolism 		3 0 3 0.18 0 0
CUI: C3160844
Disease: PAI-1 polymorphism
PAI-1 polymorphism 		10 0 4 0.17 0 0
CUI: C0751010
Disease: Cerebral Infarction, Left Hemisphere
Cerebral Infarction, Left Hemisphere 		11 0 4 0.17 0 0
CUI: C0751011
Disease: Cerebral Infarction, Right Hemisphere
Cerebral Infarction, Right Hemisphere 		11 0 4 0.17 0 0
CUI: C0751012
Disease: Anterior Choroidal Artery Infarction
Anterior Choroidal Artery Infarction 		11 0 4 0.17 0 0
CUI: C0887799
Disease: Posterior Choroidal Artery Infarction
Posterior Choroidal Artery Infarction 		11 0 4 0.17 0 0
CUI: C3805092
Disease: Methylenetetrahydrofolate reductase gene mutation
Methylenetetrahydrofolate reductase gene mutation 		11 0 4 0.17 0 0
CUI: C0242666
Disease: Protein S Deficiency
Protein S Deficiency 		19 0 5 0.16 0 0
CUI: C0600433
Disease: Activated Protein C Resistance
Activated Protein C Resistance 		41 0 8 0.16 0 0
CUI: C0238096
Disease: Embolism, Paradoxical
Embolism, Paradoxical 		5 0 3 0.16 0 0
CUI: C0852077
Disease: Blood Coagulation Disorders, Inherited
Blood Coagulation Disorders, Inherited 		5 0 3 0.16 0 0
CUI: C0936261
Disease: Brain Thrombus
Brain Thrombus 		5 0 3 0.16 0 0
CUI: C2584409
Disease: Prothrombin G20210A mutation
Prothrombin G20210A mutation 		20 0 5 0.16 0 0
CUI: C0751014
Disease: Subcortical Infarction
Subcortical Infarction 		13 0 4 0.15 0 0
CUI: C0338507
Disease: Non-arteritic ischemic optic neuropathy
Non-arteritic ischemic optic neuropathy 		6 0 3 0.15 0 0
CUI: C0584984
Disease: Heterozygous Factor V Leiden mutation
Heterozygous Factor V Leiden mutation 		6 0 3 0.15 0 0
CUI: C2609046
Disease: Sticky platelet syndrome
Sticky platelet syndrome 		6 0 3 0.15 0 0
CUI: C3160845
Disease: PAI-1 4G/5G polymorphism
PAI-1 4G/5G polymorphism 		6 0 3 0.15 0 0
CUI: C3647902
Disease: Vasculogenic erectile dysfunction
Vasculogenic erectile dysfunction 		6 3 3 0.15 1 0.11
CUI: C0795687
Disease: Cerebral arterial thrombosis
Cerebral arterial thrombosis 		14 0 4 0.15 0 0