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: C1849343
Disease: Duplication of the distal phalanx of hand
Duplication of the distal phalanx of hand 		4 0 3 0.38 0 0
CUI: C4021772
Disease: Bifid distal phalanx of toe
Bifid distal phalanx of toe 		4 0 3 0.38 0 0
CUI: C4022477
Disease: Onychogryposis of fingernail
Onychogryposis of fingernail 		4 0 3 0.38 0 0
CUI: C4551476
Disease: Robinow Syndrome, Autosomal Dominant
Robinow Syndrome, Autosomal Dominant 		4 0 3 0.38 0 0
CUI: C1854409
Disease: Naevus flammeus of the eyelid
Naevus flammeus of the eyelid 		6 0 3 0.30 0 0
CUI: C4225363
Disease: ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2 		3 0 2 0.25 0 0
CUI: C4551475
Disease: ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1 		3 0 2 0.25 0 0
CUI: C1303001
Disease: Congenital euryblepharon
Congenital euryblepharon 		9 0 3 0.23 0 0
CUI: C1849392
Disease: Ridged fingernail
Ridged fingernail 		9 0 3 0.23 0 0
CUI: C2750604
Disease: Median cleft lip and palate
Median cleft lip and palate 		15 0 4 0.22 0 0
CUI: C1865038
Disease: Broad toe
Broad toe 		11 0 3 0.20 0 0
CUI: C4020952
Disease: Fingernail dysplasia
Fingernail dysplasia 		11 0 3 0.20 0 0
CUI: C0019288
Disease: Hernia, Femoral
Hernia, Femoral 		18 0 4 0.19 0 0
CUI: C1849341
Disease: Triangular mouth
Triangular mouth 		14 0 3 0.17 0 0
CUI: C2673670
Disease: Curly eyelashes
Curly eyelashes 		15 0 3 0.16 0 0
CUI: C1442965
Disease: Avascular necrosis of the capital femoral epiphysis
Avascular necrosis of the capital femoral epiphysis 		23 0 4 0.15 0 0
CUI: C0006262
Disease: Bronchial Fistula
Bronchial Fistula 		1 0 1 0.14 0 0
CUI: C0158564
Disease: Congenital vitreous anomaly
Congenital vitreous anomaly 		1 0 1 0.14 0 0
CUI: C0231450
Disease: Abnormal extension
Abnormal extension 		1 0 1 0.14 0 0
CUI: C0233286
Disease: Frank Breech Presentation
Frank Breech Presentation 		1 1 1 0.14 1 0.25
CUI: C0265856
Disease: Hypoplasia of right heart
Hypoplasia of right heart 		1 0 1 0.14 0 0
CUI: C0268357
Disease: Osteogenesis imperfecta, type 1A
Osteogenesis imperfecta, type 1A 		1 0 1 0.14 0 0
CUI: C0426827
Disease: Gap in ribs
Gap in ribs 		1 0 1 0.14 0 0
CUI: C0701825
Disease: Acute mastoiditis
Acute mastoiditis 		1 0 1 0.14 0 0
CUI: C1834060
Disease: Short middle phalanx of the 5th finger
Short middle phalanx of the 5th finger 		17 0 3 0.14 0 0