Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Heterozygous Factor V Leiden mutation
6 0 5 0.28 0 0
CUI: C0162529
Disease: Colitis, Ischemic
Colitis, Ischemic
15 3 6 0.23 1 0.14
CUI: C2584620
Disease: Thrombophilia, hereditary
Thrombophilia, hereditary
17 9 6 0.21 3 0.27
CUI: C1260403
Disease: prothrombin gene mutation
prothrombin gene mutation
23 5 7 0.21 3 0.43
CUI: C0025297
Disease: Viral meningitis
Viral meningitis
14 0 5 0.19 0 0
CUI: C0272375
Disease: Antithrombin III Deficiency
Antithrombin III Deficiency
27 52 7 0.19 3 5.6E-02
CUI: C0398621
Disease: Hypoplasminogenemia
Hypoplasminogenemia
9 3 4 0.18 2 0.33
CUI: C3665816
Disease: Perinatal stroke
Perinatal stroke
3 0 3 0.18 0 0
CUI: C0015530
Disease: Hereditary Factor XIII Deficiency
Hereditary Factor XIII Deficiency
10 0 4 0.17 0 0
CUI: C0338573
Disease: Cerebral venous sinus thrombosis
Cerebral venous sinus thrombosis
17 1 5 0.17 1 0.20
CUI: C0265099
Disease: Basilar artery thrombosis
Basilar artery thrombosis
4 0 3 0.17 0 0
Methylenetetrahydrofolate reductase gene mutation
11 3 4 0.17 2 0.33
CUI: C0242666
Disease: Protein S Deficiency
Protein S Deficiency
19 14 5 0.16 4 0.27
Blood Coagulation Disorders, Inherited
5 0 3 0.16 0 0
CUI: C0032320
Disease: Pneumoperitoneum
Pneumoperitoneum
28 0 6 0.15 0 0
CUI: C0543822
Disease: Atherosclerotic occlusive disease
Atherosclerotic occlusive disease
13 0 4 0.15 0 0
5,10-Methylenetetrahydrofolate reductase deficiency
6 6 3 0.15 1 1.0E-01
Non-arteritic ischemic optic neuropathy
6 3 3 0.15 2 0.33
Sporadic Cerebral Amyloid Angiopathy
6 0 3 0.15 0 0
CUI: C2609046
Disease: Sticky platelet syndrome
Sticky platelet syndrome
6 2 3 0.15 1 0.17
CUI: C4316906
Disease: Factor XIII deficiency disease
Factor XIII deficiency disease
6 0 3 0.15 0 0
CUI: C4317320
Disease: Factor V deficiency
Factor V deficiency
6 0 3 0.15 0 0
CUI: C0000809
Disease: Abortion, Habitual
Abortion, Habitual
7 0 3 0.14 0 0
CUI: C0007688
Disease: Central Retinal Artery Occlusion
Central Retinal Artery Occlusion
7 0 3 0.14 0 0
CUI: C0015499
Disease: Hereditary Factor V Deficiency
Hereditary Factor V Deficiency
7 0 3 0.14 0 0