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: C0596887
Disease: mathematical ability
mathematical ability 		854 0 2 2.0E-03 0 0
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		338 0 1 2.0E-03 0 0
CUI: C1861403
Disease: Variable expressivity
Variable expressivity 		319 0 1 2.1E-03 0 0
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		272 0 1 2.4E-03 0 0
CUI: C0021704
Disease: Intelligence
Intelligence 		645 0 2 2.5E-03 0 0
CUI: C0266470
Disease: Cerebellar Hypoplasia
Cerebellar Hypoplasia 		226 0 1 2.7E-03 0 0
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies 		219 0 1 2.7E-03 0 0
CUI: C0034935
Disease: Babinski Reflex
Babinski Reflex 		218 0 1 2.7E-03 0 0
CUI: C1387005
Disease: Penis agenesis
Penis agenesis 		217 0 1 2.7E-03 0 0
CUI: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia 		216 0 1 2.7E-03 0 0
CUI: C0423109
Disease: Upward slant of palpebral fissure
Upward slant of palpebral fissure 		216 0 1 2.7E-03 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		215 0 1 2.7E-03 0 0
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		578 0 2 2.7E-03 0 0
CUI: C0333068
Disease: Flexion contracture
Flexion contracture 		210 0 1 2.8E-03 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex 		201 0 1 2.8E-03 0 0
CUI: C3494422
Disease: Retrognathia
Retrognathia 		191 0 1 2.9E-03 0 0
CUI: C0152427
Disease: Polydactyly
Polydactyly 		188 0 1 2.9E-03 0 0
CUI: C0410528
Disease: Skeletal dysplasia
Skeletal dysplasia 		186 0 1 3.0E-03 0 0
CUI: C0015469
Disease: Facial paralysis
Facial paralysis 		182 0 1 3.0E-03 0 0
CUI: C1837249
Disease: Malformations of Cortical Development, Group II
Malformations of Cortical Development, Group II 		180 0 1 3.0E-03 0 0
CUI: C0018524
Disease: Hallucinations
Hallucinations 		178 0 1 3.0E-03 0 0
CUI: C0026034
Disease: Microstomia
Microstomia 		172 0 1 3.1E-03 0 0
CUI: C0751837
Disease: Gait Ataxia
Gait Ataxia 		172 0 1 3.1E-03 0 0
CUI: C2267233
Disease: Neonatal Hypotonia
Neonatal Hypotonia 		169 0 1 3.1E-03 0 0
CUI: C0393593
Disease: Dystonia Disorders
Dystonia Disorders 		167 0 1 3.1E-03 0 0