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: C1968804
Disease: Plasminogen Deficiency, Type I
Plasminogen Deficiency, Type I 		3 0 2 8.3E-02 0 0
CUI: C2712907
Disease: obsolete Combined hyperlipidemia
obsolete Combined hyperlipidemia 		17 0 3 8.1E-02 0 0
CUI: C3549252
Disease: response to statin
response to statin 		6 8 2 7.4E-02 1 9.1E-03
CUI: C0342883
Disease: Cholesteryl Ester Transfer Protein Deficiency
Cholesteryl Ester Transfer Protein Deficiency 		22 0 3 7.1E-02 0 0
CUI: C0398621
Disease: Hypoplasminogenemia
Hypoplasminogenemia 		9 0 2 6.7E-02 0 0
CUI: C3149462
Disease: HYPERALPHALIPOPROTEINEMIA 1
HYPERALPHALIPOPROTEINEMIA 1 		9 0 2 6.7E-02 0 0
CUI: C0342880
Disease: Polygenic hypercholesterolemia
Polygenic hypercholesterolemia 		10 0 2 6.5E-02 0 0
CUI: C3888506
Disease: LDLR mutation
LDLR mutation 		10 0 2 6.5E-02 0 0
CUI: C0020479
Disease: Hyperlipoproteinemia Type III
Hyperlipoproteinemia Type III 		28 24 3 6.2E-02 1 7.9E-03
CUI: C0020480
Disease: Hyperlipoproteinemia Type IV
Hyperlipoproteinemia Type IV 		11 0 2 6.2E-02 0 0
CUI: C3805092
Disease: Methylenetetrahydrofolate reductase gene mutation
Methylenetetrahydrofolate reductase gene mutation 		11 0 2 6.2E-02 0 0
CUI: C1862596
Disease: Familial hypobetalipoproteinemia
Familial hypobetalipoproteinemia 		12 0 2 6.1E-02 0 0
CUI: C0878486
Disease: Arteriolosclerosis
Arteriolosclerosis 		13 0 2 5.9E-02 0 0
CUI: C0151945
Disease: Thrombosis of cerebral veins
Thrombosis of cerebral veins 		35 0 3 5.5E-02 0 0
CUI: C0037198
Disease: Sinus Thrombosis, Intracranial
Sinus Thrombosis, Intracranial 		17 0 2 5.3E-02 0 0
CUI: C2584620
Disease: Thrombophilia, hereditary
Thrombophilia, hereditary 		17 0 2 5.3E-02 0 0
CUI: C0263420
Disease: Hyperkeratosis lenticularis perstans
Hyperkeratosis lenticularis perstans 		18 0 2 5.1E-02 0 0
CUI: C0242666
Disease: Protein S Deficiency
Protein S Deficiency 		19 0 2 5.0E-02 0 0
CUI: C0020597
Disease: Hypobetalipoproteinemias
Hypobetalipoproteinemias 		20 0 2 4.9E-02 0 0
CUI: C0338455
Disease: Dementia of frontal lobe type
Dementia of frontal lobe type 		20 0 2 4.9E-02 0 0
CUI: C0473527
Disease: Hypoalphalipoproteinemias
Hypoalphalipoproteinemias 		20 0 2 4.9E-02 0 0
CUI: C0342882
Disease: Familial hypercholesterolemia - heterozygous
Familial hypercholesterolemia - heterozygous 		42 0 3 4.8E-02 0 0
CUI: C0276548
Disease: HIV encephalitis
HIV encephalitis 		43 0 3 4.8E-02 0 0
CUI: C0751706
Disease: Primary Progressive Nonfluent Aphasia
Primary Progressive Nonfluent Aphasia 		21 0 2 4.8E-02 0 0
CUI: C3495426
Disease: Homocysteinemia
Homocysteinemia 		21 0 2 4.8E-02 0 0