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: C0079102
Disease: Cerebral Thrombosis
Cerebral Thrombosis 		15 7 13 0.81 7 0.78
CUI: C0151945
Disease: Thrombosis of cerebral veins
Thrombosis of cerebral veins 		35 11 13 0.36 7 0.54
CUI: C3805092
Disease: Methylenetetrahydrofolate reductase gene mutation
Methylenetetrahydrofolate reductase gene mutation 		11 3 6 0.32 2 0.20
CUI: C0238457
Disease: Thrombosis of renal vein
Thrombosis of renal vein 		4 0 4 0.29 0 0
CUI: C2584620
Disease: Thrombophilia, hereditary
Thrombophilia, hereditary 		17 9 6 0.24 3 0.20
CUI: C0242666
Disease: Protein S Deficiency
Protein S Deficiency 		19 14 6 0.22 3 0.15
CUI: C2585317
Disease: Acquired thrombophilia
Acquired thrombophilia 		8 2 4 0.22 2 0.22
CUI: C0034341
Disease: Pyruvate Carboxylase Deficiency Disease
Pyruvate Carboxylase Deficiency Disease 		14 0 5 0.22 0 0
CUI: C0267412
Disease: Mesenteric Venous Thrombosis
Mesenteric Venous Thrombosis 		3 0 3 0.21 0 0
CUI: C0035302
Disease: Retinal Artery Occlusion
Retinal Artery Occlusion 		9 1 4 0.21 1 0.11
CUI: C0398621
Disease: Hypoplasminogenemia
Hypoplasminogenemia 		9 3 4 0.21 2 0.20
CUI: C1260403
Disease: prothrombin gene mutation
prothrombin gene mutation 		23 5 6 0.19 3 0.27
CUI: C0338573
Disease: Cerebral venous sinus thrombosis
Cerebral venous sinus thrombosis 		17 1 5 0.19 1 0.11
CUI: C0852077
Disease: Blood Coagulation Disorders, Inherited
Blood Coagulation Disorders, Inherited 		5 0 3 0.19 0 0
CUI: C1510431
Disease: Superficial Thrombophlebitis
Superficial Thrombophlebitis 		5 0 3 0.19 0 0
CUI: C3550150
Disease: Recurrent thrombophlebitis
Recurrent thrombophlebitis 		5 0 3 0.19 0 0
CUI: C0268615
Disease: 5,10-Methylenetetrahydrofolate reductase deficiency
5,10-Methylenetetrahydrofolate reductase deficiency 		6 6 3 0.18 1 7.1E-02
CUI: C0338507
Disease: Non-arteritic ischemic optic neuropathy
Non-arteritic ischemic optic neuropathy 		6 3 3 0.18 2 0.20
CUI: C0340517
Disease: Atrial thrombosis
Atrial thrombosis 		6 0 3 0.18 0 0
CUI: C0584984
Disease: Heterozygous Factor V Leiden mutation
Heterozygous Factor V Leiden mutation 		6 0 3 0.18 0 0
CUI: C2584409
Disease: Prothrombin G20210A mutation
Prothrombin G20210A mutation 		20 9 5 0.17 3 0.20
CUI: C0000809
Disease: Abortion, Habitual
Abortion, Habitual 		7 0 3 0.17 0 0
CUI: C0007688
Disease: Central Retinal Artery Occlusion
Central Retinal Artery Occlusion 		7 0 3 0.17 0 0
CUI: C3279439
Disease: Recurrent spontaneous abortion
Recurrent spontaneous abortion 		7 0 3 0.17 0 0
CUI: C3495426
Disease: Homocysteinemia
Homocysteinemia 		21 6 5 0.17 4 0.36