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: C0265998
Disease: ANONYCHIA
ANONYCHIA
30 0 7 0.15 0 0
Hereditary Connective Tissue Disorder
9 0 4 0.14 0 0
CUI: C1856963
Disease: Fragile nails
Fragile nails
27 0 6 0.14 0 0
CUI: C0152415
Disease: Ankyloglossia
Ankyloglossia
19 0 5 0.14 0 0
CUI: C4551650
Disease: Esophageal Stricture
Esophageal Stricture
20 0 5 0.13 0 0
CUI: C0079298
Disease: Epidermolysis Bullosa Simplex
Epidermolysis Bullosa Simplex
30 0 6 0.13 0 0
Epidermolysis Bullosa Herpetiformis Dowling-Meara
4 0 3 0.12 0 0
CUI: C0080333
Disease: Weber-Cockayne Syndrome
Weber-Cockayne Syndrome
4 0 3 0.12 0 0
CUI: C1844592
Disease: Soft skin
Soft skin
22 3 5 0.12 1 0.20
CUI: C4023812
Disease: Aplasia of the bladder
Aplasia of the bladder
4 0 3 0.12 0 0
EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 2
4 0 3 0.12 0 0
NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9
77 0 11 0.12 0 0
CUI: C0241074
Disease: Hyperextensible skin
Hyperextensible skin
50 11 8 0.12 2 0.17
CUI: C1834405
Disease: Nail dysplasia
Nail dysplasia
78 0 11 0.12 0 0
CUI: C0155760
Disease: Rupture of artery
Rupture of artery
5 0 3 0.12 0 0
Elevated maternal serum alpha-fetoprotein
5 0 3 0.12 0 0
EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 1
5 0 3 0.12 0 0
CUI: C0221260
Disease: Dystrophia unguium
Dystrophia unguium
81 0 11 0.12 0 0
CUI: C0011351
Disease: Dental Enamel Hypoplasia
Dental Enamel Hypoplasia
72 0 10 0.12 0 0
CUI: C0268338
Disease: Ehlers-Danlos Syndrome, Type IV
Ehlers-Danlos Syndrome, Type IV
7 0 3 0.11 0 0
CUI: C1844738
Disease: Axillary pterygium
Axillary pterygium
7 0 3 0.11 0 0
Epidermolysis bullosa with pyloric atresia
7 0 3 0.11 0 0
CUI: C4551676
Disease: Laryngismus stridulus
Laryngismus stridulus
7 0 3 0.11 0 0
CUI: C1851789
Disease: Poor wound healing
Poor wound healing
19 0 4 0.11 0 0
CUI: C3814530
Disease: Skin Vesicle
Skin Vesicle
20 0 4 0.10 0 0