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: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 1 0.25
CUI: C1314691
Disease: Age at menarche
Age at menarche 		267 0 1 1.8E-03 0 0
CUI: C1854882
Disease: Absent speech
Absent speech 		232 0 1 1.9E-03 0 0
CUI: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia 		216 0 1 1.9E-03 0 0
CUI: C0423109
Disease: Upward slant of palpebral fissure
Upward slant of palpebral fissure 		216 0 1 1.9E-03 0 0
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios 		208 0 1 2.0E-03 0 0
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy 		187 0 1 2.0E-03 0 0
CUI: C1837249
Disease: Malformations of Cortical Development, Group II
Malformations of Cortical Development, Group II 		180 0 1 2.1E-03 0 0
CUI: C1854113
Disease: Prominent nasal bridge
Prominent nasal bridge 		180 0 1 2.1E-03 0 0
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement 		169 0 1 2.1E-03 0 0
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate 		169 0 1 2.1E-03 0 0
CUI: C1853743
Disease: Muscular hypotonia of the trunk
Muscular hypotonia of the trunk 		156 0 1 2.2E-03 0 0
CUI: C0037769
Disease: West Syndrome
West Syndrome 		149 0 1 2.2E-03 0 0
CUI: C0004106
Disease: Astigmatism
Astigmatism 		148 0 1 2.2E-03 0 0
CUI: C1858430
Disease: Death in infancy
Death in infancy 		146 0 1 2.2E-03 0 0
CUI: C0231686
Disease: Gait, Unsteady
Gait, Unsteady 		143 0 1 2.2E-03 0 0
CUI: C0393525
Disease: Progressive cerebellar ataxia
Progressive cerebellar ataxia 		136 0 1 2.3E-03 0 0
CUI: C4048268
Disease: Cortical visual impairment
Cortical visual impairment 		136 0 1 2.3E-03 0 0
CUI: C0423113
Disease: Telecanthus
Telecanthus 		134 0 1 2.3E-03 0 0
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		131 0 1 2.3E-03 0 0
CUI: C0018498
Disease: Hair Color
Hair Color 		130 0 1 2.3E-03 0 0
CUI: C1837397
Disease: Severe global developmental delay
Severe global developmental delay 		130 0 1 2.3E-03 0 0
CUI: C0266483
Disease: Pachygyria
Pachygyria 		129 0 1 2.3E-03 0 0
CUI: C0266544
Disease: Microcornea
Microcornea 		129 0 1 2.3E-03 0 0
CUI: C0240543
Disease: Bulbous nose
Bulbous nose 		123 0 1 2.3E-03 0 0