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: C0026034
Disease: Microstomia
Microstomia 		172 0 1 3.5E-03 0 0
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement 		169 0 1 3.6E-03 0 0
CUI: C2267233
Disease: Neonatal Hypotonia
Neonatal Hypotonia 		169 0 1 3.6E-03 0 0
CUI: C0008489
Disease: Chorea
Chorea 		168 0 1 3.6E-03 0 0
CUI: C1854494
Disease: Slow progression
Slow progression 		165 0 1 3.6E-03 0 0
CUI: C4025790
Disease: Specific learning disability
Specific learning disability 		165 0 1 3.6E-03 0 0
CUI: C0038379
Disease: Strabismus
Strabismus 		716 0 3 3.6E-03 0 0
CUI: C0162298
Disease: Joint stiffness
Joint stiffness 		163 0 1 3.6E-03 0 0
CUI: C0020796
Disease: Profound Mental Retardation
Profound Mental Retardation 		160 0 1 3.7E-03 0 0
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		160 0 1 3.7E-03 0 0
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding) 		160 0 1 3.7E-03 0 0
CUI: C1837260
Disease: Prominent forehead
Prominent forehead 		159 0 1 3.7E-03 0 0
CUI: C0234132
Disease: Pyramidal sign
Pyramidal sign 		155 0 1 3.8E-03 0 0
CUI: C0024433
Disease: Macrostomia
Macrostomia 		148 0 1 3.9E-03 0 0
CUI: C0917816
Disease: Mental deficiency
Mental deficiency 		148 0 1 3.9E-03 0 0
CUI: C1858430
Disease: Death in infancy
Death in infancy 		146 0 1 3.9E-03 0 0
CUI: C1839739
Disease: Thick lower lip vermilion
Thick lower lip vermilion 		145 0 1 3.9E-03 0 0
CUI: C0009171
Disease: Cocaine Abuse
Cocaine Abuse 		144 0 1 3.9E-03 0 0
CUI: C0037772
Disease: Spastic Paraplegia
Spastic Paraplegia 		144 0 1 3.9E-03 0 0
CUI: C0021704
Disease: Intelligence
Intelligence 		645 0 3 4.0E-03 0 0
CUI: C0037369
Disease: Smoking
Smoking 		391 0 2 4.0E-03 0 0
CUI: C0005938
Disease: Bone Density
Bone Density 		138 0 1 4.0E-03 0 0
CUI: C3714758
Disease: Juvenile psoriatic arthritis
Juvenile psoriatic arthritis 		138 0 1 4.0E-03 0 0
CUI: C0393525
Disease: Progressive cerebellar ataxia
Progressive cerebellar ataxia 		136 0 1 4.0E-03 0 0
CUI: C1998028
Disease: Photoreceptor degeneration
Photoreceptor degeneration 		136 0 1 4.0E-03 0 0