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: C1836038
Disease: Poor head control
Poor head control 		162 0 1 3.4E-03 0 0
CUI: C1837260
Disease: Prominent forehead
Prominent forehead 		159 0 1 3.4E-03 0 0
CUI: C1853743
Disease: Muscular hypotonia of the trunk
Muscular hypotonia of the trunk 		156 0 1 3.4E-03 0 0
CUI: C0005890
Disease: Body Height
Body Height 		1903 0 7 3.4E-03 0 0
CUI: C0004106
Disease: Astigmatism
Astigmatism 		148 0 1 3.5E-03 0 0
CUI: C2700617
Disease: Irritation - emotion
Irritation - emotion 		147 0 1 3.5E-03 0 0
CUI: C1858430
Disease: Death in infancy
Death in infancy 		146 0 1 3.6E-03 0 0
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		145 0 1 3.6E-03 0 0
CUI: C1839739
Disease: Thick lower lip vermilion
Thick lower lip vermilion 		145 0 1 3.6E-03 0 0
CUI: C0231686
Disease: Gait, Unsteady
Gait, Unsteady 		143 0 1 3.6E-03 0 0
CUI: C0020490
Disease: Hyperopia
Hyperopia 		142 0 1 3.6E-03 0 0
CUI: C0022107
Disease: Irritable Mood
Irritable Mood 		142 0 1 3.6E-03 0 0
CUI: C4552810
Disease: Irritability, CTCAE
Irritability, CTCAE 		140 0 1 3.6E-03 0 0
CUI: C0003466
Disease: Anus, Imperforate
Anus, Imperforate 		139 0 1 3.6E-03 0 0
CUI: C0158731
Disease: Congenital pectus carinatum
Congenital pectus carinatum 		138 0 1 3.7E-03 0 0
CUI: C0152423
Disease: Congenital small ears
Congenital small ears 		137 0 1 3.7E-03 0 0
CUI: C1963094
Disease: Dry Skin, CTCAE
Dry Skin, CTCAE 		137 0 1 3.7E-03 0 0
CUI: C0393525
Disease: Progressive cerebellar ataxia
Progressive cerebellar ataxia 		136 0 1 3.7E-03 0 0
CUI: C0038271
Disease: Stereotyped Behavior
Stereotyped Behavior 		135 0 1 3.7E-03 0 0
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		135 0 1 3.7E-03 0 0
CUI: C0423113
Disease: Telecanthus
Telecanthus 		134 0 1 3.7E-03 0 0
CUI: C0233565
Disease: Bradykinesia
Bradykinesia 		133 0 1 3.7E-03 0 0
CUI: C1849089
Disease: Broad forehead
Broad forehead 		133 0 1 3.7E-03 0 0
CUI: C1837397
Disease: Severe global developmental delay
Severe global developmental delay 		130 0 1 3.8E-03 0 0
CUI: C0265660
Disease: Syndactyly of the toes
Syndactyly of the toes 		129 0 1 3.8E-03 0 0