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: C1963184
Disease: Nystagmus, CTCAE 3.0
Nystagmus, CTCAE 3.0 		779 0 120 0.12 0 0
CUI: C4554036
Disease: Nystagmus, CTCAE 5.0
Nystagmus, CTCAE 5.0 		779 0 120 0.12 0 0
CUI: C0079924
Disease: Oligohydramnios
Oligohydramnios 		129 21 50 0.12 1 1.7E-02
CUI: C0028738
Disease: Nystagmus
Nystagmus 		833 95 121 0.12 2 1.5E-02
CUI: C1861866
Disease: Aplasia/Hypoplasia of the corpus callosum
Aplasia/Hypoplasia of the corpus callosum 		108 0 46 0.12 0 0
CUI: C0265660
Disease: Syndactyly of the toes
Syndactyly of the toes 		129 0 48 0.11 0 0
CUI: C0175754
Disease: Agenesis of corpus callosum
Agenesis of corpus callosum 		615 45 98 0.11 1 1.2E-02
CUI: C4024748
Disease: Aplasia/Hypoplasia of the iris
Aplasia/Hypoplasia of the iris 		52 0 40 0.11 0 0
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease 		384 0 74 0.11 0 0
CUI: C0014065
Disease: Congenital cerebral hernia
Congenital cerebral hernia 		93 0 44 0.11 0 0
CUI: C1857486
Disease: Low-set, posteriorly rotated ears
Low-set, posteriorly rotated ears 		223 0 57 0.11 0 0
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		274 0 62 0.11 0 0
CUI: C0013274
Disease: Patent ductus arteriosus
Patent ductus arteriosus 		510 56 85 0.11 1 1.1E-02
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		850 135 119 0.11 3 1.7E-02
CUI: C1836735
Disease: hypopigmented skin patch
hypopigmented skin patch 		123 0 46 0.11 0 0
CUI: C1850049
Disease: Clinodactyly of the 5th finger
Clinodactyly of the 5th finger 		284 0 61 0.11 0 0
CUI: C2919142
Disease: Short Stature, CTCAE
Short Stature, CTCAE 		1010 0 132 0.11 0 0
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis 		595 0 91 0.11 0 0
CUI: C0033377
Disease: Ptosis
Ptosis 		607 0 92 0.11 0 0
CUI: C0029124
Disease: Optic Atrophy
Optic Atrophy 		568 51 87 0.11 2 2.2E-02
CUI: C3278923
Disease: Dilated ventricles (finding)
Dilated ventricles (finding) 		427 32 72 0.10 1 1.4E-02
CUI: C1306710
Disease: Facial asymmetry
Facial asymmetry 		109 13 42 0.10 2 3.9E-02
CUI: C1531647
Disease: Cerebral ventriculomegaly
Cerebral ventriculomegaly 		410 0 70 0.10 0 0
CUI: C1849367
Disease: Nasal bridge wide
Nasal bridge wide 		429 0 71 0.10 0 0
CUI: C1306503
Disease: Congenital exomphalos
Congenital exomphalos 		235 0 53 0.10 0 0