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: C3495426
Disease: Homocysteinemia
Homocysteinemia 		21 6 8 0.20 1 8.1E-03
CUI: C0019880
Disease: Homocystinuria
Homocystinuria 		39 27 10 0.18 22 0.18
CUI: C4048705
Disease: Hypermethioninemia
Hypermethioninemia 		16 3 6 0.16 1 8.3E-03
CUI: C3805092
Disease: Methylenetetrahydrofolate reductase gene mutation
Methylenetetrahydrofolate reductase gene mutation 		11 3 5 0.15 1 8.3E-03
CUI: C0795687
Disease: Cerebral arterial thrombosis
Cerebral arterial thrombosis 		14 9 5 0.14 1 7.9E-03
CUI: C0079102
Disease: Cerebral Thrombosis
Cerebral Thrombosis 		15 7 5 0.14 1 8.1E-03
CUI: C0268621
Disease: Hepatic methionine adenosyltransferase deficiency
Hepatic methionine adenosyltransferase deficiency 		16 15 5 0.13 1 7.6E-03
CUI: C0338573
Disease: Cerebral venous sinus thrombosis
Cerebral venous sinus thrombosis 		17 1 5 0.13 1 8.5E-03
CUI: C1273976
Disease: First myocardial infarction
First myocardial infarction 		17 0 5 0.13 0 0
CUI: C2584620
Disease: Thrombophilia, hereditary
Thrombophilia, hereditary 		17 9 5 0.13 1 7.9E-03
CUI: C0035302
Disease: Retinal Artery Occlusion
Retinal Artery Occlusion 		9 1 4 0.12 1 8.5E-03
CUI: C0936215
Disease: Vitamin B 6 Deficiency
Vitamin B 6 Deficiency 		11 0 4 0.12 0 0
CUI: C3806347
Disease: Hyperhomocystinemia
Hyperhomocystinemia 		11 0 4 0.12 0 0
CUI: C1260403
Disease: prothrombin gene mutation
prothrombin gene mutation 		23 5 5 0.11 1 8.2E-03
CUI: C0151945
Disease: Thrombosis of cerebral veins
Thrombosis of cerebral veins 		35 11 6 0.11 1 7.8E-03
CUI: C0040038
Disease: Thromboembolism
Thromboembolism 		25 0 5 0.11 0 0
CUI: C0852077
Disease: Blood Coagulation Disorders, Inherited
Blood Coagulation Disorders, Inherited 		5 0 3 0.10 0 0
CUI: C0037198
Disease: Sinus Thrombosis, Intracranial
Sinus Thrombosis, Intracranial 		17 5 4 1.0E-01 1 8.2E-03
CUI: C0268615
Disease: 5,10-Methylenetetrahydrofolate reductase deficiency
5,10-Methylenetetrahydrofolate reductase deficiency 		6 0 3 1.0E-01 0 0
CUI: C0338507
Disease: Non-arteritic ischemic optic neuropathy
Non-arteritic ischemic optic neuropathy 		6 3 3 1.0E-01 1 8.3E-03
CUI: C0340517
Disease: Atrial thrombosis
Atrial thrombosis 		6 0 3 1.0E-01 0 0
CUI: C0584984
Disease: Heterozygous Factor V Leiden mutation
Heterozygous Factor V Leiden mutation 		6 0 3 1.0E-01 0 0
CUI: C0000809
Disease: Abortion, Habitual
Abortion, Habitual 		7 0 3 9.7E-02 0 0
CUI: C0393561
Disease: Subcortical Vascular Dementia
Subcortical Vascular Dementia 		8 0 3 9.4E-02 0 0
CUI: C2585317
Disease: Acquired thrombophilia
Acquired thrombophilia 		8 2 3 9.4E-02 1 8.4E-03