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: C1857569
Disease: CORNEAL ENDOTHELIAL DYSTROPHY 2
CORNEAL ENDOTHELIAL DYSTROPHY 2 		9 24 6 0.67 7 0.26
CUI: C1562689
Disease: Congenital hereditary endothelial dystrophy
Congenital hereditary endothelial dystrophy 		5 0 4 0.57 0 0
CUI: C1857572
Disease: CORNEAL DYSTROPHY AND PERCEPTIVE DEAFNESS
CORNEAL DYSTROPHY AND PERCEPTIVE DEAFNESS 		3 0 3 0.50 0 0
CUI: C1857800
Disease: CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 2
CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 2 		6 0 4 0.50 0 0
CUI: C1852555
Disease: CORNEAL ENDOTHELIAL DYSTROPHY 1, AUTOSOMAL DOMINANT
CORNEAL ENDOTHELIAL DYSTROPHY 1, AUTOSOMAL DOMINANT 		12 0 5 0.38 0 0
CUI: C0271288
Disease: Corneal guttata
Corneal guttata 		6 0 3 0.33 0 0
CUI: C0339284
Disease: Polymorphous corneal dystrophy
Polymorphous corneal dystrophy 		14 0 5 0.33 0 0
CUI: C0474444
Disease: Corneal stromal edema
Corneal stromal edema 		2 0 2 0.33 0 0
CUI: C0155116
Disease: Descemet's membrane fold
Descemet's membrane fold 		1 0 1 0.17 0 0
CUI: C0178282
Disease: Hernia of abdominal cavity
Hernia of abdominal cavity 		1 0 1 0.17 0 0
CUI: C0474441
Disease: Fine corneal edema
Fine corneal edema 		1 0 1 0.17 0 0
CUI: C1563274
Disease: Congenital hereditary endothelial dystrophy,CHED 2
Congenital hereditary endothelial dystrophy,CHED 2 		1 0 1 0.17 0 0
CUI: C1836724
Disease: CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 3 (disorder)
CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 3 (disorder) 		1 0 1 0.17 0 0
CUI: C1852795
Disease: CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 2
CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 2 		1 0 1 0.17 0 0
CUI: C2750448
Disease: CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 6
CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 6 		1 0 1 0.17 0 0
CUI: C2750450
Disease: CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 4
CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 4 		1 11 1 0.17 1 5.0E-02
CUI: C4479246
Disease: CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER
CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER 		1 0 1 0.17 0 0
CUI: C0238157
Disease: Benign hematuria
Benign hematuria 		2 0 1 0.14 0 0
CUI: C1611195
Disease: Congenital corneal dystrophy
Congenital corneal dystrophy 		2 0 1 0.14 0 0
CUI: C1850048
Disease: Absent proximal finger flexion creases
Absent proximal finger flexion creases 		2 0 1 0.14 0 0
CUI: C1856644
Disease: Absent/hypoplastic coccyx
Absent/hypoplastic coccyx 		2 0 1 0.14 0 0
CUI: C2751480
Disease: Hypoplastic coccygeal vertebrae
Hypoplastic coccygeal vertebrae 		2 0 1 0.14 0 0
CUI: C2931253
Disease: Alport syndrome, dominant type
Alport syndrome, dominant type 		2 0 1 0.14 0 0
CUI: C2931861
Disease: Hemorrhagic hereditary nephritis
Hemorrhagic hereditary nephritis 		2 0 1 0.14 0 0
CUI: C3554462
Disease: MITOCHONDRIAL DNA DEPLETION SYNDROME 11
MITOCHONDRIAL DNA DEPLETION SYNDROME 11 		2 0 1 0.14 0 0