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: C0272322
Disease: Severe hereditary factor VIII deficiency disease
Severe hereditary factor VIII deficiency disease 		37 15 7 0.11 4 0.24
CUI: C0272375
Disease: Antithrombin III Deficiency
Antithrombin III Deficiency 		27 52 6 0.11 4 7.4E-02
CUI: C0472803
Disease: Hypodysfibrinogenemia
Hypodysfibrinogenemia 		8 0 4 0.11 0 0
CUI: C0398621
Disease: Hypoplasminogenemia
Hypoplasminogenemia 		9 3 4 0.11 2 0.29
CUI: C2584409
Disease: Prothrombin G20210A mutation
Prothrombin G20210A mutation 		20 9 5 0.10 3 0.25
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		117 218 14 0.10 1 4.5E-03
CUI: C3160844
Disease: PAI-1 polymorphism
PAI-1 polymorphism 		10 0 4 0.10 0 0
CUI: C0751010
Disease: Cerebral Infarction, Left Hemisphere
Cerebral Infarction, Left Hemisphere 		11 0 4 1.0E-01 0 0
CUI: C0751011
Disease: Cerebral Infarction, Right Hemisphere
Cerebral Infarction, Right Hemisphere 		11 0 4 1.0E-01 0 0
CUI: C0751012
Disease: Anterior Choroidal Artery Infarction
Anterior Choroidal Artery Infarction 		11 0 4 1.0E-01 0 0
CUI: C0887799
Disease: Posterior Choroidal Artery Infarction
Posterior Choroidal Artery Infarction 		11 0 4 1.0E-01 0 0
CUI: C0948441
Disease: Venoocclusive disease
Venoocclusive disease 		34 4 6 9.8E-02 1 0.11
CUI: C0003838
Disease: Arterial Occlusive Diseases
Arterial Occlusive Diseases 		35 4 6 9.7E-02 3 0.43
CUI: C1963943
Disease: Atherothrombosis
Atherothrombosis 		115 15 13 9.6E-02 2 0.11
CUI: C0751014
Disease: Subcortical Infarction
Subcortical Infarction 		13 0 4 9.5E-02 0 0
CUI: C1412000
Disease: Mesenteric vascular insufficiency
Mesenteric vascular insufficiency 		13 0 4 9.5E-02 0 0
CUI: C0034341
Disease: Pyruvate Carboxylase Deficiency Disease
Pyruvate Carboxylase Deficiency Disease 		14 0 4 9.3E-02 0 0
CUI: C0795687
Disease: Cerebral arterial thrombosis
Cerebral arterial thrombosis 		14 9 4 9.3E-02 3 0.25
CUI: C2717961
Disease: Thrombotic Microangiopathies
Thrombotic Microangiopathies 		62 8 8 9.2E-02 2 0.17
CUI: C0013922
Disease: Embolism
Embolism 		3 0 3 9.1E-02 0 0
CUI: C0019880
Disease: Homocystinuria
Homocystinuria 		39 0 6 9.1E-02 0 0
CUI: C0085278
Disease: Antiphospholipid Syndrome
Antiphospholipid Syndrome 		99 17 11 9.1E-02 3 0.15
CUI: C0751202
Disease: Cystathionine beta-Synthase Deficiency Disease
Cystathionine beta-Synthase Deficiency Disease 		27 118 5 9.1E-02 1 8.1E-03
CUI: C0238457
Disease: Thrombosis of renal vein
Thrombosis of renal vein 		4 0 3 8.8E-02 0 0
CUI: C1867596
Disease: Hyperprothrombinemia
Hyperprothrombinemia 		4 0 3 8.8E-02 0 0