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: C0600433
Disease: Activated Protein C Resistance
Activated Protein C Resistance 		41 30 11 0.17 3 9.7E-02
CUI: C0340170
Disease: Complicated pneumoconiosis
Complicated pneumoconiosis 		13 0 6 0.15 0 0
CUI: C0034341
Disease: Pyruvate Carboxylase Deficiency Disease
Pyruvate Carboxylase Deficiency Disease 		14 0 6 0.14 0 0
CUI: C4225412
Disease: Spondylo-ocular syndrome
Spondylo-ocular syndrome 		24 0 7 0.14 0 0
CUI: C2584620
Disease: Thrombophilia, hereditary
Thrombophilia, hereditary 		17 9 6 0.13 2 0.18
CUI: C3160844
Disease: PAI-1 polymorphism
PAI-1 polymorphism 		10 0 5 0.13 0 0
CUI: C0242666
Disease: Protein S Deficiency
Protein S Deficiency 		19 14 6 0.13 2 0.12
CUI: C0019156
Disease: Hepatic Veno-Occlusive Disease
Hepatic Veno-Occlusive Disease 		37 0 8 0.13 0 0
CUI: C0031736
Disease: Polymorphous light eruption
Polymorphous light eruption 		20 0 6 0.12 0 0
CUI: C1827377
Disease: Slow acetylator due to N-acetyltransferase enzyme variant
Slow acetylator due to N-acetyltransferase enzyme variant 		20 0 6 0.12 0 0
CUI: C3805092
Disease: Methylenetetrahydrofolate reductase gene mutation
Methylenetetrahydrofolate reductase gene mutation 		11 0 5 0.12 0 0
CUI: C1260403
Disease: prothrombin gene mutation
prothrombin gene mutation 		23 5 6 0.12 2 0.29
CUI: C0277919
Disease: Postthrombotic Syndrome
Postthrombotic Syndrome 		14 0 5 0.12 0 0
CUI: C0238096
Disease: Embolism, Paradoxical
Embolism, Paradoxical 		5 0 4 0.11 0 0
CUI: C0079102
Disease: Cerebral Thrombosis
Cerebral Thrombosis 		15 7 5 0.11 1 1.0E-01
CUI: C0267809
Disease: Cirrhosis, Cryptogenic
Cirrhosis, Cryptogenic 		15 5 5 0.11 1 0.12
CUI: C0584960
Disease: Factor V Leiden mutation
Factor V Leiden mutation 		86 46 12 0.11 3 6.4E-02
CUI: C1273976
Disease: First myocardial infarction
First myocardial infarction 		17 0 5 0.11 0 0
CUI: C0007688
Disease: Central Retinal Artery Occlusion
Central Retinal Artery Occlusion 		7 0 4 0.11 0 0
CUI: C0524688
Disease: Pneumonic Plague
Pneumonic Plague 		8 0 4 0.11 0 0
CUI: C1709735
Disease: Prosthetic Valve Thrombosis
Prosthetic Valve Thrombosis 		8 0 4 0.11 0 0
CUI: C0019087
Disease: Hemorrhagic Disorders
Hemorrhagic Disorders 		30 0 6 0.10 0 0
CUI: C0398621
Disease: Hypoplasminogenemia
Hypoplasminogenemia 		9 0 4 0.10 0 0
CUI: C2880562
Disease: Age-related cortical cataract
Age-related cortical cataract 		9 0 4 0.10 0 0
CUI: C2584409
Disease: Prothrombin G20210A mutation
Prothrombin G20210A mutation 		20 9 5 0.10 2 0.18