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: C1306503
Disease: Congenital exomphalos
Congenital exomphalos 		235 0 1 1.5E-03 0 0
CUI: C0086437
Disease: Joint laxity
Joint laxity 		224 0 1 1.6E-03 0 0
CUI: C0311394
Disease: Difficulty walking
Difficulty walking 		224 0 1 1.6E-03 0 0
CUI: C1857486
Disease: Low-set, posteriorly rotated ears
Low-set, posteriorly rotated ears 		223 0 1 1.6E-03 0 0
CUI: C0020608
Disease: Hypodontia
Hypodontia 		218 0 1 1.6E-03 0 0
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios 		208 0 1 1.6E-03 0 0
CUI: C0040420
Disease: Tonometry
Tonometry 		206 0 1 1.6E-03 0 0
CUI: C0038273
Disease: Stereotypic Movement Disorder
Stereotypic Movement Disorder 		192 0 1 1.7E-03 0 0
CUI: C0152427
Disease: Polydactyly
Polydactyly 		188 0 1 1.7E-03 0 0
CUI: C1854113
Disease: Prominent nasal bridge
Prominent nasal bridge 		180 0 1 1.7E-03 0 0
CUI: C0431478
Disease: Posteriorly rotated ear
Posteriorly rotated ear 		176 0 1 1.7E-03 0 0
CUI: C0026034
Disease: Microstomia
Microstomia 		172 0 1 1.7E-03 0 0
CUI: C0221352
Disease: Syndactyly of fingers
Syndactyly of fingers 		171 0 1 1.7E-03 0 0
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement 		169 0 1 1.7E-03 0 0
CUI: C2267233
Disease: Neonatal Hypotonia
Neonatal Hypotonia 		169 0 1 1.7E-03 0 0
CUI: C0409348
Disease: Flexion contracture of proximal interphalangeal joint
Flexion contracture of proximal interphalangeal joint 		168 0 1 1.7E-03 0 0
CUI: C0020796
Disease: Profound Mental Retardation
Profound Mental Retardation 		160 0 1 1.8E-03 0 0
CUI: C1837260
Disease: Prominent forehead
Prominent forehead 		159 0 1 1.8E-03 0 0
CUI: C0684276
Disease: Hypsarrhythmia
Hypsarrhythmia 		152 0 1 1.8E-03 0 0
CUI: C1855285
Disease: Protruding ear
Protruding ear 		152 0 1 1.8E-03 0 0
CUI: C1857679
Disease: Sloping forehead
Sloping forehead 		149 0 1 1.8E-03 0 0
CUI: C0004106
Disease: Astigmatism
Astigmatism 		148 0 1 1.8E-03 0 0
CUI: C0917816
Disease: Mental deficiency
Mental deficiency 		148 0 1 1.8E-03 0 0
CUI: C1839739
Disease: Thick lower lip vermilion
Thick lower lip vermilion 		145 0 1 1.8E-03 0 0
CUI: C0424678
Disease: Lean body mass
Lean body mass 		144 0 1 1.8E-03 0 0