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: C0234182
Disease: Gowers sign
Gowers sign 		54 0 1 1.7E-03 0 0
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders 		54 0 1 1.7E-03 0 0
CUI: C1278049
Disease: Serum gamma-glutamyl transferase measurement
Serum gamma-glutamyl transferase measurement 		54 0 1 1.7E-03 0 0
CUI: C4021219
Disease: Multifocal epileptiform discharges
Multifocal epileptiform discharges 		52 0 1 1.7E-03 0 0
CUI: C0233523
Disease: Antisocial behavior
Antisocial behavior 		51 0 1 1.7E-03 0 0
CUI: C0239067
Disease: Difficulty walking up stairs
Difficulty walking up stairs 		51 0 1 1.7E-03 0 0
CUI: C0282201
Disease: Phosphate Diabetes
Phosphate Diabetes 		51 0 1 1.7E-03 0 0
CUI: C0455988
Disease: Hydrops Fetalis, Non-Immune
Hydrops Fetalis, Non-Immune 		51 0 1 1.7E-03 0 0
CUI: C2677180
Disease: Congenital microcephaly
Congenital microcephaly 		51 0 1 1.7E-03 0 0
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders 		50 0 1 1.7E-03 0 0
CUI: C0427144
Disease: Toe-walking gait
Toe-walking gait 		50 0 1 1.7E-03 0 0
CUI: C1843700
Disease: Increased variability in muscle fiber diameter
Increased variability in muscle fiber diameter 		50 0 1 1.7E-03 0 0
CUI: C0240479
Disease: Neck muscle weakness
Neck muscle weakness 		49 0 1 1.7E-03 0 0
CUI: C0271385
Disease: Horizontal Nystagmus
Horizontal Nystagmus 		48 0 1 1.7E-03 0 0
CUI: C0401149
Disease: Chronic constipation
Chronic constipation 		47 0 1 1.7E-03 0 0
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic 		46 0 1 1.7E-03 0 0
CUI: C1136179
Disease: Hammer Toe
Hammer Toe 		46 0 1 1.7E-03 0 0
CUI: C4024926
Disease: Focal T2 hyperintense basal ganglia lesion
Focal T2 hyperintense basal ganglia lesion 		46 0 1 1.7E-03 0 0
CUI: C0271093
Disease: Stargardt's disease
Stargardt's disease 		45 0 1 1.7E-03 0 0
CUI: C1837402
Disease: Flat occiput
Flat occiput 		45 0 1 1.7E-03 0 0
CUI: C2112129
Disease: Postaxial foot polydactyly
Postaxial foot polydactyly 		45 0 1 1.7E-03 0 0
CUI: C0015930
Disease: Fetal Distress
Fetal Distress 		44 0 1 1.7E-03 0 0
CUI: C0332615
Disease: Myopathic facies
Myopathic facies 		44 0 1 1.7E-03 0 0
CUI: C0427055
Disease: Facial Paresis
Facial Paresis 		44 0 1 1.7E-03 0 0
CUI: C0546967
Disease: Posterior embryotoxon
Posterior embryotoxon 		44 0 1 1.7E-03 0 0