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: C1853738
Disease: Long eyelashes
Long eyelashes 		83 0 14 0.17 0 0
CUI: C0266383
Disease: Uterine Anomalies
Uterine Anomalies 		35 0 7 0.16 0 0
CUI: C4023918
Disease: Short hard palate
Short hard palate 		7 0 3 0.16 0 0
CUI: C2750604
Disease: Median cleft lip and palate
Median cleft lip and palate 		15 0 4 0.15 0 0
CUI: C4551560
Disease: Truncal obesity
Truncal obesity 		38 0 7 0.15 0 0
CUI: C1842366
Disease: Low anterior hairline
Low anterior hairline 		71 0 11 0.15 0 0
CUI: C0270972
Disease: Cornelia De Lange Syndrome
Cornelia De Lange Syndrome 		48 0 8 0.15 0 0
CUI: C0042961
Disease: Intestinal Volvulus
Intestinal Volvulus 		42 0 7 0.14 0 0
CUI: C0019288
Disease: Hernia, Femoral
Hernia, Femoral 		18 0 4 0.14 0 0
CUI: C1866190
Disease: Atresia of the external auditory canal
Atresia of the external auditory canal 		44 0 7 0.13 0 0
CUI: C2673653
Disease: Cuboid-shaped vertebral bodies
Cuboid-shaped vertebral bodies 		2 0 2 0.13 0 0
CUI: C4225164
Disease: ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3 		2 0 2 0.13 0 0
CUI: C1865038
Disease: Broad toe
Broad toe 		11 0 3 0.13 0 0
CUI: C0265205
Disease: Robinow Syndrome
Robinow Syndrome 		20 0 4 0.13 0 0
CUI: C1269700
Disease: Caliectasis
Caliectasis 		3 0 2 0.12 0 0
CUI: C1847363
Disease: Aplasia/Hypoplasia of the ribs
Aplasia/Hypoplasia of the ribs 		3 0 2 0.12 0 0
CUI: C4551475
Disease: ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1 		3 0 2 0.12 0 0
CUI: C0795905
Disease: Cantu syndrome
Cantu syndrome 		4 0 2 0.12 0 0
CUI: C1442965
Disease: Avascular necrosis of the capital femoral epiphysis
Avascular necrosis of the capital femoral epiphysis 		23 0 4 0.12 0 0
CUI: C1849341
Disease: Triangular mouth
Triangular mouth 		14 0 3 0.12 0 0
CUI: C0266111
Disease: Bifid tongue
Bifid tongue 		24 0 4 0.11 0 0
CUI: C0005741
Disease: Blepharitis
Blepharitis 		55 0 7 0.11 0 0
CUI: C0235864
Disease: Congenital hypertrichosis lanuginosa
Congenital hypertrichosis lanuginosa 		6 0 2 0.11 0 0
CUI: C2936812
Disease: Congenital hypertrichosis
Congenital hypertrichosis 		6 0 2 0.11 0 0
CUI: C1834060
Disease: Short middle phalanx of the 5th finger
Short middle phalanx of the 5th finger 		17 0 3 0.10 0 0