Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Pyruvate Carboxylase Deficiency Disease
14 0 11 0.12 0 0
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
378 408 51 0.12 24 5.6E-02
CUI: C0085409
Disease: Polyendocrinopathies, Autoimmune
Polyendocrinopathies, Autoimmune
166 21 27 0.12 1 1.5E-02
CUI: C0338573
Disease: Cerebral venous sinus thrombosis
Cerebral venous sinus thrombosis
17 1 11 0.12 1 2.2E-02
CUI: C0087086
Disease: Thrombus
Thrombus
46 0 14 0.12 0 0
Methylenetetrahydrofolate reductase gene mutation
11 3 10 0.11 2 4.3E-02
CUI: C0042974
Disease: von Willebrand Disease
von Willebrand Disease
62 78 15 0.11 4 3.3E-02
CUI: C0019154
Disease: Hepatic Vein Thrombosis
Hepatic Vein Thrombosis
23 4 11 0.11 4 8.7E-02
CUI: C0019069
Disease: Hemophilia A
Hemophilia A
143 295 23 0.11 5 1.5E-02
CUI: C0856761
Disease: Budd-Chiari Syndrome
Budd-Chiari Syndrome
24 4 11 0.11 4 8.7E-02
CUI: C0948441
Disease: Venoocclusive disease
Venoocclusive disease
34 4 12 0.11 3 6.4E-02
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
267 31 35 0.11 6 8.5E-02
CUI: C0040015
Disease: Thrombasthenia
Thrombasthenia
48 61 13 0.11 3 2.9E-02
CUI: C3495426
Disease: Homocysteinemia
Homocysteinemia
21 6 10 0.10 6 0.13
CUI: C0085096
Disease: Peripheral Vascular Diseases
Peripheral Vascular Diseases
150 18 22 0.10 4 6.7E-02
CUI: C1260903
Disease: Dysfibrinogenemia
Dysfibrinogenemia
13 6 9 1.0E-01 1 2.0E-02
Peripheral arterial occlusive disease
35 3 11 1.0E-01 2 4.3E-02
CUI: C3845502
Disease: Myocardial infarction, stroke
Myocardial infarction, stroke
46 0 12 1.0E-01 0 0
Purpura, Thrombotic Thrombocytopenic
80 0 15 9.9E-02 0 0
CUI: C0040038
Disease: Thromboembolism
Thromboembolism
25 0 10 9.9E-02 0 0
CUI: C0034065
Disease: Pulmonary Embolism
Pulmonary Embolism
93 16 16 9.8E-02 2 3.3E-02
CUI: C0079102
Disease: Cerebral Thrombosis
Cerebral Thrombosis
15 7 9 9.8E-02 4 8.2E-02
CUI: C1273976
Disease: First myocardial infarction
First myocardial infarction
17 0 9 9.6E-02 0 0
CUI: C0598608
Disease: Hyperhomocysteinemia
Hyperhomocysteinemia
246 45 29 9.6E-02 11 0.14
Premature coronary artery atherosclerosis
87 43 15 9.5E-02 1 1.1E-02