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: C4551705
Disease: Abnormality of chromosome stability
Abnormality of chromosome stability 		34 0 23 0.14 0 0
CUI: C0238093
Disease: Stenosis of duodenum
Stenosis of duodenum 		29 0 22 0.14 0 0
CUI: C0008297
Disease: Choanal Atresia
Choanal Atresia 		104 0 31 0.14 0 0
CUI: C0240635
Disease: Byzanthine arch palate
Byzanthine arch palate 		497 70 78 0.14 4 4.3E-02
CUI: C0151640
Disease: Decreased fertility in males
Decreased fertility in males 		30 0 22 0.14 0 0
CUI: C3887489
Disease: Clubbing of toes
Clubbing of toes 		30 0 22 0.14 0 0
CUI: C0241397
Disease: Triphalangeal thumb
Triphalangeal thumb 		56 0 25 0.14 0 0
CUI: C4025211
Disease: Abnormal carotid artery morphology
Abnormal carotid artery morphology 		32 0 22 0.13 0 0
CUI: C1963099
Disease: Myelodysplasia, CTCAE
Myelodysplasia, CTCAE 		68 0 26 0.13 0 0
CUI: C0221352
Disease: Syndactyly of fingers
Syndactyly of fingers 		171 0 38 0.13 0 0
CUI: C2749463
Disease: Aplasia/Hypoplasia of the radius
Aplasia/Hypoplasia of the radius 		45 0 23 0.13 0 0
CUI: C0239676
Disease: High forehead
High forehead 		211 17 42 0.13 1 2.4E-02
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism 		725 80 100 0.13 1 9.5E-03
CUI: C0025990
Disease: Micrognathism
Micrognathism 		586 53 84 0.13 2 2.6E-02
CUI: C4024748
Disease: Aplasia/Hypoplasia of the iris
Aplasia/Hypoplasia of the iris 		52 0 23 0.13 0 0
CUI: C0040588
Disease: Tracheoesophageal Fistula
Tracheoesophageal Fistula 		80 0 26 0.12 0 0
CUI: C0266387
Disease: Bicornuate uterus
Bicornuate uterus 		44 0 22 0.12 0 0
CUI: C0025037
Disease: Meckel Diverticulum
Meckel Diverticulum 		63 0 24 0.12 0 0
CUI: C0020534
Disease: Orbital separation excessive
Orbital separation excessive 		590 77 82 0.12 3 3.0E-02
CUI: C0079924
Disease: Oligohydramnios
Oligohydramnios 		129 21 31 0.12 1 2.2E-02
CUI: C2674432
Disease: Reduced bone mineral density
Reduced bone mineral density 		76 0 25 0.12 0 0
CUI: C2267233
Disease: Neonatal Hypotonia
Neonatal Hypotonia 		169 45 35 0.12 3 4.4E-02
CUI: C0151311
Disease: Cranial nerve palsies
Cranial nerve palsies 		81 0 25 0.12 0 0
CUI: C1836735
Disease: hypopigmented skin patch
hypopigmented skin patch 		123 0 29 0.12 0 0
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects 		384 96 56 0.12 3 2.5E-02