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: C0020623
Disease: Hypolipoproteinemias
Hypolipoproteinemias 		1 0 1 1.00 0 0
CUI: C0035326
Disease: Retinal vascular occlusion
Retinal vascular occlusion 		1 0 1 1.00 0 0
CUI: C0276044
Disease: Contagious bovine pleuropneumonia
Contagious bovine pleuropneumonia 		1 0 1 1.00 0 0
CUI: C0339495
Disease: Cilioretinal artery occlusion
Cilioretinal artery occlusion 		1 0 1 1.00 0 0
CUI: C1720772
Disease: Hypoprebetalipoproteinemia
Hypoprebetalipoproteinemia 		1 0 1 1.00 0 0
CUI: C1735914
Disease: Recurrent pulmonary embolism
Recurrent pulmonary embolism 		2 0 1 0.50 0 0
CUI: C0333184
Disease: Calcific stenosis
Calcific stenosis 		3 0 1 0.33 0 0
CUI: C0741032
Disease: Refractory angina
Refractory angina 		3 0 1 0.33 0 0
CUI: C1968804
Disease: Plasminogen Deficiency, Type I
Plasminogen Deficiency, Type I 		3 0 1 0.33 0 0
CUI: C3665816
Disease: Perinatal stroke
Perinatal stroke 		3 0 1 0.33 0 0
CUI: C0267839
Disease: Hepatic amyloidosis
Hepatic amyloidosis 		4 0 1 0.25 0 0
CUI: C4274665
Disease: Logopenic progressive aphasia
Logopenic progressive aphasia 		4 0 1 0.25 0 0
CUI: C3875011
Disease: Familial hyperalphalipoproteinemia
Familial hyperalphalipoproteinemia 		5 0 1 0.20 0 0
CUI: C0584984
Disease: Heterozygous Factor V Leiden mutation
Heterozygous Factor V Leiden mutation 		6 0 1 0.17 0 0
CUI: C3549252
Disease: response to statin
response to statin 		6 0 1 0.17 0 0
CUI: C4316906
Disease: Factor XIII deficiency disease
Factor XIII deficiency disease 		6 0 1 0.17 0 0
CUI: C0007688
Disease: Central Retinal Artery Occlusion
Central Retinal Artery Occlusion 		7 0 1 0.14 0 0
CUI: C0155567
Disease: Rheumatic aortic stenosis
Rheumatic aortic stenosis 		7 0 1 0.14 0 0
CUI: C0342879
Disease: Primary hypercholesterolemia
Primary hypercholesterolemia 		7 0 1 0.14 0 0
CUI: C0282529
Disease: Chondrodysplasia Punctata, Rhizomelic
Chondrodysplasia Punctata, Rhizomelic 		8 0 1 0.12 0 0
CUI: C0919718
Disease: Calcification of mitral valve
Calcification of mitral valve 		8 0 1 0.12 0 0
CUI: C0302892
Disease: Congenital porencephaly
Congenital porencephaly 		9 0 1 0.11 0 0
CUI: C0398621
Disease: Hypoplasminogenemia
Hypoplasminogenemia 		9 0 1 0.11 0 0
CUI: C4082173
Disease: Porencephaly
Porencephaly 		9 0 1 0.11 0 0
CUI: C0015530
Disease: Hereditary Factor XIII Deficiency
Hereditary Factor XIII Deficiency 		10 0 1 1.0E-01 0 0