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: C0584984
Disease: Heterozygous Factor V Leiden mutation
Heterozygous Factor V Leiden mutation 		6 0 4 0.40 0 0
CUI: C1510431
Disease: Superficial Thrombophlebitis
Superficial Thrombophlebitis 		5 0 3 0.30 0 0
CUI: C0339499
Disease: Central retinal vein occlusion - juvenile
Central retinal vein occlusion - juvenile 		2 0 2 0.25 0 0
CUI: C0795832
Disease: Chromosome 9, tetrasomy 9p
Chromosome 9, tetrasomy 9p 		2 0 2 0.25 0 0
CUI: C1610621
Disease: Factor II mutation
Factor II mutation 		2 0 2 0.25 0 0
CUI: C1861171
Disease: THROMBOPHILIA DUE TO ACTIVATED PROTEIN C RESISTANCE (disorder)
THROMBOPHILIA DUE TO ACTIVATED PROTEIN C RESISTANCE (disorder) 		2 0 2 0.25 0 0
CUI: C2585684
Disease: Heterozygous prothrombin G20210A mutation
Heterozygous prothrombin G20210A mutation 		2 0 2 0.25 0 0
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		3 0 2 0.22 0 0
CUI: C3665816
Disease: Perinatal stroke
Perinatal stroke 		3 0 2 0.22 0 0
CUI: C0162529
Disease: Colitis, Ischemic
Colitis, Ischemic 		15 0 4 0.21 0 0
CUI: C0238457
Disease: Thrombosis of renal vein
Thrombosis of renal vein 		4 0 2 0.20 0 0
CUI: C0553576
Disease: Systemic mycosis
Systemic mycosis 		4 0 2 0.20 0 0
CUI: C1527411
Disease: Thrombosis of retinal vein
Thrombosis of retinal vein 		4 0 2 0.20 0 0
CUI: C2584620
Disease: Thrombophilia, hereditary
Thrombophilia, hereditary 		17 0 4 0.19 0 0
CUI: C0852077
Disease: Blood Coagulation Disorders, Inherited
Blood Coagulation Disorders, Inherited 		5 0 2 0.18 0 0
CUI: C0268615
Disease: 5,10-Methylenetetrahydrofolate reductase deficiency
5,10-Methylenetetrahydrofolate reductase deficiency 		6 0 2 0.17 0 0
CUI: C0338507
Disease: Non-arteritic ischemic optic neuropathy
Non-arteritic ischemic optic neuropathy 		6 0 2 0.17 0 0
CUI: C0034341
Disease: Pyruvate Carboxylase Deficiency Disease
Pyruvate Carboxylase Deficiency Disease 		14 0 3 0.16 0 0
CUI: C0000809
Disease: Abortion, Habitual
Abortion, Habitual 		7 0 2 0.15 0 0
CUI: C0007688
Disease: Central Retinal Artery Occlusion
Central Retinal Artery Occlusion 		7 0 2 0.15 0 0
CUI: C0750145
Disease: Occlusive vascular disease
Occlusive vascular disease 		7 0 2 0.15 0 0
CUI: C0085650
Disease: Purpura Fulminans
Purpura Fulminans 		15 0 3 0.15 0 0
CUI: C1260403
Disease: prothrombin gene mutation
prothrombin gene mutation 		23 0 4 0.15 0 0
CUI: C2585317
Disease: Acquired thrombophilia
Acquired thrombophilia 		8 0 2 0.14 0 0
CUI: C0037198
Disease: Sinus Thrombosis, Intracranial
Sinus Thrombosis, Intracranial 		17 0 3 0.14 0 0