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: C1314691
Disease: Age at menarche
Age at menarche 		267 0 1 2.1E-03 0 0
CUI: C0266435
Disease: Congenital hypoplasia of penis
Congenital hypoplasia of penis 		237 0 1 2.2E-03 0 0
CUI: C0034935
Disease: Babinski Reflex
Babinski Reflex 		218 0 1 2.3E-03 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		215 0 1 2.3E-03 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex 		201 0 1 2.4E-03 0 0
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy 		190 0 1 2.5E-03 0 0
CUI: C0221356
Disease: Brachycephaly
Brachycephaly 		186 0 1 2.5E-03 0 0
CUI: C1861324
Disease: Short philtrum
Short philtrum 		182 0 1 2.5E-03 0 0
CUI: C0026034
Disease: Microstomia
Microstomia 		172 0 1 2.6E-03 0 0
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement 		169 0 1 2.6E-03 0 0
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity 		147 0 1 2.7E-03 0 0
CUI: C1858430
Disease: Death in infancy
Death in infancy 		146 0 1 2.8E-03 0 0
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		145 0 1 2.8E-03 0 0
CUI: C0037772
Disease: Spastic Paraplegia
Spastic Paraplegia 		144 0 1 2.8E-03 0 0
CUI: C0231686
Disease: Gait, Unsteady
Gait, Unsteady 		143 0 1 2.8E-03 0 0
CUI: C0152423
Disease: Congenital small ears
Congenital small ears 		137 0 1 2.8E-03 0 0
CUI: C0393525
Disease: Progressive cerebellar ataxia
Progressive cerebellar ataxia 		136 0 1 2.8E-03 0 0
CUI: C1848673
Disease: Hypoplastic feet
Hypoplastic feet 		129 0 1 2.9E-03 0 0
CUI: C0236969
Disease: Substance-Related Disorders
Substance-Related Disorders 		128 0 1 2.9E-03 0 0
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		124 0 1 2.9E-03 0 0
CUI: C1842876
Disease: Depressed nasal ridge
Depressed nasal ridge 		117 0 1 3.0E-03 0 0
CUI: C0576226
Disease: Short foot
Short foot 		116 0 1 3.0E-03 0 0
CUI: C3665386
Disease: Abnormal vision
Abnormal vision 		115 0 1 3.0E-03 0 0
CUI: C0010038
Disease: Corneal Opacity
Corneal Opacity 		113 0 1 3.0E-03 0 0
CUI: C1849211
Disease: Generalized hirsutism
Generalized hirsutism 		113 0 1 3.0E-03 0 0