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: C0266298
Disease: Accessory kidney
Accessory kidney 		20 0 13 0.17 0 0
CUI: C0080174
Disease: Spina Bifida Occulta
Spina Bifida Occulta 		76 0 20 0.16 0 0
CUI: C0266061
Disease: Open Bite
Open Bite 		38 0 14 0.15 0 0
CUI: C0265886
Disease: Overriding aorta
Overriding aorta 		17 0 11 0.15 0 0
CUI: C0235752
Disease: Port-Wine Stain
Port-Wine Stain 		46 0 14 0.14 0 0
CUI: C0376480
Disease: Gingival Overgrowth
Gingival Overgrowth 		100 0 19 0.13 0 0
CUI: C4021801
Disease: Lacrimation abnormality
Lacrimation abnormality 		29 0 11 0.13 0 0
CUI: C1837279
Disease: Hypoplastic toenails
Hypoplastic toenails 		42 0 12 0.12 0 0
CUI: C0546967
Disease: Posterior embryotoxon
Posterior embryotoxon 		44 0 12 0.12 0 0
CUI: C1853738
Disease: Long eyelashes
Long eyelashes 		83 0 16 0.12 0 0
CUI: C4024897
Disease: Atrophy/Degeneration involving the corticospinal tracts
Atrophy/Degeneration involving the corticospinal tracts 		8 0 8 0.12 0 0
CUI: C0005744
Disease: Blepharophimosis
Blepharophimosis 		106 0 18 0.11 0 0
CUI: C4022386
Disease: Overfriendliness
Overfriendliness 		9 0 8 0.11 0 0
CUI: C4025788
Disease: Nystagmus-induced head nodding
Nystagmus-induced head nodding 		9 0 8 0.11 0 0
CUI: C4025898
Disease: Functional abnormality of male internal genitalia
Functional abnormality of male internal genitalia 		9 0 8 0.11 0 0
CUI: C4023752
Disease: Abnormality of the diencephalon
Abnormality of the diencephalon 		10 0 8 0.11 0 0
CUI: C4023676
Disease: Increased nuchal translucency
Increased nuchal translucency 		30 0 10 0.11 0 0
CUI: C0332606
Disease: Elfin facies
Elfin facies 		11 0 8 0.11 0 0
CUI: C1866134
Disease: Wide anterior fontanel
Wide anterior fontanel 		71 5 14 0.11 1 6.7E-02
CUI: C4025362
Disease: Abnormality of the gastric mucosa
Abnormality of the gastric mucosa 		12 0 8 0.11 0 0
CUI: C1850049
Disease: Clinodactyly of the 5th finger
Clinodactyly of the 5th finger 		284 39 34 0.11 2 4.2E-02
CUI: C0344530
Disease: Congenital keratoglobus
Congenital keratoglobus 		46 0 11 0.11 0 0
CUI: C0158761
Disease: Radioulnar Synostosis
Radioulnar Synostosis 		67 0 13 0.11 0 0
CUI: C0426891
Disease: Broad thumbs
Broad thumbs 		67 11 13 0.11 1 4.8E-02
CUI: C0221209
Disease: Pelvic kidney
Pelvic kidney 		15 0 8 0.11 0 0