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: C4021050
Disease: Dilated superficial abdominal veins
Dilated superficial abdominal veins
3 0 2 0.20 0 0
CUI: C4022766
Disease: Abnormal large intestine physiology
Abnormal large intestine physiology
3 0 2 0.20 0 0
Elevated alkaline phosphatase of hepatic origin
3 0 2 0.20 0 0
CUI: C4022867
Disease: Spider hemangioma
Spider hemangioma
4 0 2 0.18 0 0
CUI: C4020948
Disease: Palmar telangiectasia
Palmar telangiectasia
5 0 2 0.17 0 0
CUI: C4025612
Disease: Polyclonal elevation of IgM
Polyclonal elevation of IgM
5 0 2 0.17 0 0
CUI: C0271288
Disease: Corneal guttata
Corneal guttata
6 0 2 0.15 0 0
CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 2
6 0 2 0.15 0 0
CUI: C0342895
Disease: Fish-Eye Disease
Fish-Eye Disease
19 0 3 0.12 0 0
CUI: C4699184
Disease: Fuchs
Fuchs
10 0 2 0.12 0 0
CUI: C0003708
Disease: Arachnoiditis
Arachnoiditis
1 0 1 0.11 0 0
CUI: C0155116
Disease: Descemet's membrane fold
Descemet's membrane fold
1 0 1 0.11 0 0
Epithelial basement membrane dystrophy
1 0 1 0.11 0 0
CUI: C0339271
Disease: Salzmann nodular dystrophy
Salzmann nodular dystrophy
1 0 1 0.11 0 0
CUI: C0474441
Disease: Fine corneal edema
Fine corneal edema
1 1 1 0.11 1 0.14
Corneal dystrophy, epithelial basement membrane
1 0 1 0.11 0 0
Congenital Nephrogenic Diabetes Insipidus
11 0 2 0.11 0 0
CUI: C1266156
Disease: Multicystic mesothelioma, benign
Multicystic mesothelioma, benign
1 0 1 0.11 0 0
Groenouw corneal dystrophy type I (disorder)
1 0 1 0.11 0 0
Corneal Dystrophy, Lattice Type IIIA
1 0 1 0.11 0 0
CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 2
1 2 1 0.11 2 0.29
Severe hereditary factor VIII deficiency disease without inhibitor
1 0 1 0.11 0 0
CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 3
1 0 1 0.11 0 0
CUI: C4024792
Disease: Nodular corneal dystrophy
Nodular corneal dystrophy
1 0 1 0.11 0 0
CUI: C4024796
Disease: Punctate corneal dystrophy
Punctate corneal dystrophy
1 0 1 0.11 0 0