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: C0524702
Disease: Pulmonary Thromboembolisms
Pulmonary Thromboembolisms
23 6 7 0.15 3 0.21
CUI: C0037198
Disease: Sinus Thrombosis, Intracranial
Sinus Thrombosis, Intracranial
16 5 6 0.15 2 0.14
CUI: C0035328
Disease: Retinal Vein Occlusion
Retinal Vein Occlusion
64 15 12 0.14 6 0.30
CUI: C0023234
Disease: Legg-Calve-Perthes Disease
Legg-Calve-Perthes Disease
17 0 6 0.14 0 0
CUI: C1273976
Disease: First myocardial infarction
First myocardial infarction
17 0 6 0.14 0 0
CUI: C0154841
Disease: Central retinal vein occlusion
Central retinal vein occlusion
37 7 8 0.13 2 0.12
CUI: C3805089
Disease: Hyperfibrinolysis
Hyperfibrinolysis
12 0 5 0.13 0 0
CUI: C0238457
Disease: Thrombosis of renal vein
Thrombosis of renal vein
4 0 4 0.13 0 0
CUI: C1260903
Disease: Dysfibrinogenemia
Dysfibrinogenemia
13 0 5 0.13 0 0
Cystathionine beta-Synthase Deficiency Disease
25 12 6 0.12 1 4.5E-02
CUI: C0151950
Disease: Deep thrombophlebitis
Deep thrombophlebitis
16 0 5 0.12 0 0
Peripheral arterial occlusive disease
35 3 7 0.12 2 0.17
CUI: C0398623
Disease: Thrombophilia
Thrombophilia
149 43 19 0.12 6 0.12
CUI: C0019087
Disease: Hemorrhagic Disorders
Hemorrhagic Disorders
26 0 6 0.12 0 0
CUI: C0035302
Disease: Retinal Artery Occlusion
Retinal Artery Occlusion
7 1 4 0.12 1 9.1E-02
CUI: C0019880
Disease: Homocystinuria
Homocystinuria
36 0 7 0.12 0 0
CUI: C0085278
Disease: Antiphospholipid Syndrome
Antiphospholipid Syndrome
89 11 12 0.11 2 1.0E-01
CUI: C0409980
Disease: Primary antiphospholipid syndrome
Primary antiphospholipid syndrome
29 0 6 0.11 0 0
CUI: C2608079
Disease: WARFARIN SENSITIVITY (disorder)
WARFARIN SENSITIVITY (disorder)
9 0 4 0.11 0 0
CUI: C3160844
Disease: PAI-1 polymorphism
PAI-1 polymorphism
10 0 4 0.11 0 0
CUI: C0948441
Disease: Venoocclusive disease
Venoocclusive disease
34 4 6 0.10 1 7.1E-02
CUI: C0852949
Disease: Arteriopathic disease
Arteriopathic disease
101 14 12 1.0E-01 2 8.7E-02
CUI: C0339505
Disease: Venous retinal branch occlusion
Venous retinal branch occlusion
25 7 5 9.8E-02 3 0.20
CUI: C2314994
Disease: Infarction of spinal cord
Infarction of spinal cord
14 1 4 9.8E-02 1 9.1E-02
Severe hereditary factor VIII deficiency disease
37 15 6 9.7E-02 3 0.13