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: C0856761
Disease: Budd-Chiari Syndrome
Budd-Chiari Syndrome 		24 4 22 0.88 4 1.00
CUI: C0003838
Disease: Arterial Occlusive Diseases
Arterial Occlusive Diseases 		35 4 3 5.5E-02 3 0.60
CUI: C0037198
Disease: Sinus Thrombosis, Intracranial
Sinus Thrombosis, Intracranial 		17 5 3 8.1E-02 3 0.50
CUI: C0155773
Disease: Portal Vein Thrombosis
Portal Vein Thrombosis 		59 8 12 0.17 4 0.50
CUI: C1096458
Disease: Vascular occlusion
Vascular occlusion 		30 2 5 0.10 2 0.50
CUI: C1260403
Disease: prothrombin gene mutation
prothrombin gene mutation 		23 5 6 0.15 3 0.50
CUI: C2585317
Disease: Acquired thrombophilia
Acquired thrombophilia 		8 2 4 0.15 2 0.50
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis 		15 2 3 8.6E-02 2 0.50
CUI: C4302205
Disease: Neonatal thrombosis of cerebral venous sinus
Neonatal thrombosis of cerebral venous sinus 		1 2 1 4.3E-02 2 0.50
CUI: C2584620
Disease: Thrombophilia, hereditary
Thrombophilia, hereditary 		17 9 6 0.18 4 0.44
CUI: C1852242
Disease: Nonarteritic anterior ischemic optic neuropathy (NAION)
Nonarteritic anterior ischemic optic neuropathy (NAION) 		22 6 4 9.8E-02 3 0.43
CUI: C0338507
Disease: Non-arteritic ischemic optic neuropathy
Non-arteritic ischemic optic neuropathy 		6 3 3 0.12 2 0.40
CUI: C0398621
Disease: Hypoplasminogenemia
Hypoplasminogenemia 		9 3 4 0.14 2 0.40
CUI: C2945695
Disease: Limb ischemia
Limb ischemia 		171 3 4 2.1E-02 2 0.40
CUI: C3160845
Disease: PAI-1 4G/5G polymorphism
PAI-1 4G/5G polymorphism 		6 3 1 3.6E-02 2 0.40
CUI: C3805092
Disease: Methylenetetrahydrofolate reductase gene mutation
Methylenetetrahydrofolate reductase gene mutation 		11 3 5 0.17 2 0.40
CUI: C4552318
Disease: Gastrointestinal adenocarcinoma
Gastrointestinal adenocarcinoma 		9 3 1 3.2E-02 2 0.40
CUI: C0339505
Disease: Venous retinal branch occlusion
Venous retinal branch occlusion 		25 7 4 9.1E-02 3 0.38
CUI: C2721734
Disease: Methylenetetrahydrofolate reductase polymorphism
Methylenetetrahydrofolate reductase polymorphism 		9 7 3 0.10 3 0.38
CUI: C2584409
Disease: Prothrombin G20210A mutation
Prothrombin G20210A mutation 		20 9 4 0.10 3 0.30
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism 		0 5 0 0 2 0.29
CUI: C0035328
Disease: Retinal Vein Occlusion
Retinal Vein Occlusion 		76 15 8 8.8E-02 4 0.27
CUI: C0002890
Disease: Leukoerythroblastic Anemia
Leukoerythroblastic Anemia 		1 1 1 4.3E-02 1 0.25
CUI: C0007868
Disease: Cervical dysplasia
Cervical dysplasia 		56 1 1 1.3E-02 1 0.25
CUI: C0009812
Disease: Constitutional Symptom
Constitutional Symptom 		30 1 2 3.9E-02 1 0.25