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: C3806347
Disease: Hyperhomocystinemia
Hyperhomocystinemia 		11 0 9 0.22 0 0
CUI: C0600433
Disease: Activated Protein C Resistance
Activated Protein C Resistance 		41 0 13 0.19 0 0
CUI: C0398625
Disease: Protein C Deficiency
Protein C Deficiency 		43 0 13 0.19 0 0
CUI: C0242666
Disease: Protein S Deficiency
Protein S Deficiency 		19 0 9 0.18 0 0
CUI: C0751202
Disease: Cystathionine beta-Synthase Deficiency Disease
Cystathionine beta-Synthase Deficiency Disease 		27 118 10 0.18 22 0.18
CUI: C1260403
Disease: prothrombin gene mutation
prothrombin gene mutation 		23 0 9 0.17 0 0
CUI: C3805092
Disease: Methylenetetrahydrofolate reductase gene mutation
Methylenetetrahydrofolate reductase gene mutation 		11 0 7 0.16 0 0
CUI: C1848580
Disease: Decreased methionine synthase activity
Decreased methionine synthase activity 		6 1 6 0.15 1 3.7E-02
CUI: C4021736
Disease: Decreased methylcobalamin
Decreased methylcobalamin 		7 0 6 0.15 0 0
CUI: C0272375
Disease: Antithrombin III Deficiency
Antithrombin III Deficiency 		27 0 8 0.14 0 0
CUI: C0584960
Disease: Factor V Leiden mutation
Factor V Leiden mutation 		86 0 15 0.14 0 0
CUI: C3495426
Disease: Homocysteinemia
Homocysteinemia 		21 0 7 0.13 0 0
CUI: C1848555
Disease: Hypomethioninemia
Hypomethioninemia 		5 0 5 0.13 0 0
CUI: C0034341
Disease: Pyruvate Carboxylase Deficiency Disease
Pyruvate Carboxylase Deficiency Disease 		14 0 6 0.13 0 0
CUI: C1855119
Disease: Methylmalonic aciduria
Methylmalonic aciduria 		33 0 8 0.12 0 0
CUI: C1848556
Disease: Decreased adenosylcobalamin
Decreased adenosylcobalamin 		7 0 5 0.12 0 0
CUI: C0002888
Disease: Anemia, Megaloblastic
Anemia, Megaloblastic 		26 0 7 0.12 0 0
CUI: C0338573
Disease: Cerebral venous sinus thrombosis
Cerebral venous sinus thrombosis 		17 0 6 0.12 0 0
CUI: C0272322
Disease: Severe hereditary factor VIII deficiency disease
Severe hereditary factor VIII deficiency disease 		37 0 8 0.12 0 0
CUI: C0268583
Disease: Methylmalonic acidemia
Methylmalonic acidemia 		44 0 8 0.11 0 0
CUI: C1260903
Disease: Dysfibrinogenemia
Dysfibrinogenemia 		13 0 5 0.11 0 0
CUI: C0003838
Disease: Arterial Occlusive Diseases
Arterial Occlusive Diseases 		35 0 7 0.10 0 0
CUI: C0151945
Disease: Thrombosis of cerebral veins
Thrombosis of cerebral veins 		35 0 7 0.10 0 0
CUI: C0040038
Disease: Thromboembolism
Thromboembolism 		25 0 6 0.10 0 0
CUI: C0079102
Disease: Cerebral Thrombosis
Cerebral Thrombosis 		15 0 5 0.10 0 0