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: C1260403
Disease: prothrombin gene mutation
prothrombin gene mutation 		23 5 12 0.32 4 7.5E-02
CUI: C0242666
Disease: Protein S Deficiency
Protein S Deficiency 		19 14 11 0.31 6 1.0E-01
CUI: C2584620
Disease: Thrombophilia, hereditary
Thrombophilia, hereditary 		17 9 10 0.29 4 7.0E-02
CUI: C0600433
Disease: Activated Protein C Resistance
Activated Protein C Resistance 		41 30 14 0.26 5 6.5E-02
CUI: C0398625
Disease: Protein C Deficiency
Protein C Deficiency 		43 14 14 0.25 4 6.5E-02
CUI: C0034341
Disease: Pyruvate Carboxylase Deficiency Disease
Pyruvate Carboxylase Deficiency Disease 		14 0 8 0.24 0 0
CUI: C3805092
Disease: Methylenetetrahydrofolate reductase gene mutation
Methylenetetrahydrofolate reductase gene mutation 		11 3 7 0.23 2 3.8E-02
CUI: C0584984
Disease: Heterozygous Factor V Leiden mutation
Heterozygous Factor V Leiden mutation 		6 0 6 0.22 0 0
CUI: C2584409
Disease: Prothrombin G20210A mutation
Prothrombin G20210A mutation 		20 9 8 0.21 4 7.0E-02
CUI: C0037198
Disease: Sinus Thrombosis, Intracranial
Sinus Thrombosis, Intracranial 		17 5 7 0.19 3 5.6E-02
CUI: C1510431
Disease: Superficial Thrombophlebitis
Superficial Thrombophlebitis 		5 0 5 0.19 0 0
CUI: C0007688
Disease: Central Retinal Artery Occlusion
Central Retinal Artery Occlusion 		7 0 5 0.17 0 0
CUI: C0151945
Disease: Thrombosis of cerebral veins
Thrombosis of cerebral veins 		35 11 9 0.17 3 5.0E-02
CUI: C2585317
Disease: Acquired thrombophilia
Acquired thrombophilia 		8 2 5 0.17 2 3.8E-02
CUI: C0272322
Disease: Severe hereditary factor VIII deficiency disease
Severe hereditary factor VIII deficiency disease 		37 15 9 0.16 5 8.1E-02
CUI: C0311370
Disease: Lupus anticoagulant disorder
Lupus anticoagulant disorder 		66 14 13 0.16 4 6.5E-02
CUI: C1837899
Disease: Type I transferrin isoform profile
Type I transferrin isoform profile 		16 0 6 0.16 0 0
CUI: C0398621
Disease: Hypoplasminogenemia
Hypoplasminogenemia 		9 3 5 0.16 2 3.8E-02
CUI: C0338573
Disease: Cerebral venous sinus thrombosis
Cerebral venous sinus thrombosis 		17 1 6 0.16 1 1.9E-02
CUI: C0584960
Disease: Factor V Leiden mutation
Factor V Leiden mutation 		86 46 15 0.15 6 6.5E-02
CUI: C1260903
Disease: Dysfibrinogenemia
Dysfibrinogenemia 		13 6 5 0.14 1 1.8E-02
CUI: C0795687
Disease: Cerebral arterial thrombosis
Cerebral arterial thrombosis 		14 9 5 0.14 3 5.2E-02
CUI: C0019880
Disease: Homocystinuria
Homocystinuria 		39 0 8 0.14 0 0
CUI: C0268615
Disease: 5,10-Methylenetetrahydrofolate reductase deficiency
5,10-Methylenetetrahydrofolate reductase deficiency 		6 6 4 0.14 2 3.6E-02
CUI: C0079102
Disease: Cerebral Thrombosis
Cerebral Thrombosis 		15 7 5 0.14 3 5.4E-02