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: C0340648
Disease: dissection of coronary artery
dissection of coronary artery 		1 0 1 9.1E-02 0 0
CUI: C0343287
Disease: Thoracic discitis
Thoracic discitis 		1 0 1 9.1E-02 0 0
CUI: C0344688
Disease: Patent Ductus Venosus
Patent Ductus Venosus 		1 0 1 9.1E-02 0 0
CUI: C0423262
Disease: Corneal endotheliitis
Corneal endotheliitis 		1 0 1 9.1E-02 0 0
CUI: C0423463
Disease: Opticociliary vessels
Opticociliary vessels 		1 0 1 9.1E-02 0 0
CUI: C0474354
Disease: Optic disc neovascularization
Optic disc neovascularization 		1 0 1 9.1E-02 0 0
CUI: C0521570
Disease: Retinal arteriovenous malformation
Retinal arteriovenous malformation 		1 0 1 9.1E-02 0 0
CUI: C0553577
Disease: Post-tuberculous reactive arthritis
Post-tuberculous reactive arthritis 		1 0 1 9.1E-02 0 0
CUI: C0570855
Disease: Allergy to chlorpromazine
Allergy to chlorpromazine 		1 0 1 9.1E-02 0 0
CUI: C0730274
Disease: Vitreomacular traction syndrome
Vitreomacular traction syndrome 		1 0 1 9.1E-02 0 0
CUI: C0730275
Disease: Macular pseudohole
Macular pseudohole 		1 0 1 9.1E-02 0 0
CUI: C0746779
Disease: nausea chronic
nausea chronic 		1 0 1 9.1E-02 0 0
CUI: C0856835
Disease: Seronegative juvenile chronic arthritis
Seronegative juvenile chronic arthritis 		1 0 1 9.1E-02 0 0
CUI: C0857406
Disease: Diabetic neovascularization
Diabetic neovascularization 		1 0 1 9.1E-02 0 0
CUI: C1832250
Disease: OBESITY, MODIFIER OF
OBESITY, MODIFIER OF 		1 0 1 9.1E-02 0 0
CUI: C1832251
Disease: BODY MASS INDEX, MODIFIER OF
BODY MASS INDEX, MODIFIER OF 		1 0 1 9.1E-02 0 0
CUI: C1832253
Disease: INTIMAL MEDIAL THICKNESS OF INTERNAL CAROTID ARTERY, MODIFIER OF
INTIMAL MEDIAL THICKNESS OF INTERNAL CAROTID ARTERY, MODIFIER OF 		1 0 1 9.1E-02 0 0
CUI: C1836302
Disease: Carotid Intimal Medial Thickness 1
Carotid Intimal Medial Thickness 1 		1 0 1 9.1E-02 0 0
CUI: C1856441
Disease: Late onset congenital glaucoma
Late onset congenital glaucoma 		1 0 1 9.1E-02 0 0
CUI: C1859995
Disease: Hyperandrogenism, Nonclassic Type, due to 21-Hydroxylase Deficiency
Hyperandrogenism, Nonclassic Type, due to 21-Hydroxylase Deficiency 		1 0 1 9.1E-02 0 0
CUI: C1859998
Disease: CARCINOMA, ADRENOCORTICAL, ANDROGEN-SECRETING
CARCINOMA, ADRENOCORTICAL, ANDROGEN-SECRETING 		1 1 1 9.1E-02 1 7.1E-02
CUI: C3151153
Disease: ADENOMA, CORTISOL-PRODUCING
ADENOMA, CORTISOL-PRODUCING 		1 1 1 9.1E-02 1 7.1E-02
CUI: C3241919
Disease: Erythema Multiforme Major
Erythema Multiforme Major 		1 0 1 9.1E-02 0 0
CUI: C3277286
Disease: HYPERSENSITIVITY SYNDROME, CARBAMAZEPINE-INDUCED, SUSCEPTIBILITY TO
HYPERSENSITIVITY SYNDROME, CARBAMAZEPINE-INDUCED, SUSCEPTIBILITY TO 		1 0 1 9.1E-02 0 0
CUI: C3278153
Disease: GLAUCOMA, PRIMARY OPEN ANGLE, JUVENILE-ONSET
GLAUCOMA, PRIMARY OPEN ANGLE, JUVENILE-ONSET 		1 0 1 9.1E-02 0 0