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: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders 		54 0 1 2.2E-03 0 0
CUI: C1278049
Disease: Serum gamma-glutamyl transferase measurement
Serum gamma-glutamyl transferase measurement 		54 0 1 2.2E-03 0 0
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement 		54 0 1 2.2E-03 0 0
CUI: C0017979
Disease: Glycosuria
Glycosuria 		53 0 1 2.2E-03 0 0
CUI: C0018051
Disease: Gonadal Dysgenesis
Gonadal Dysgenesis 		53 0 1 2.2E-03 0 0
CUI: C0337443
Disease: Sodium measurement
Sodium measurement 		53 0 1 2.2E-03 0 0
CUI: C1860816
Disease: Preauricular skin tag
Preauricular skin tag 		53 0 1 2.2E-03 0 0
CUI: C4021219
Disease: Multifocal epileptiform discharges
Multifocal epileptiform discharges 		52 0 1 2.2E-03 0 0
CUI: C0239067
Disease: Difficulty walking up stairs
Difficulty walking up stairs 		51 0 1 2.2E-03 0 0
CUI: C0427149
Disease: Gait, Drop Foot
Gait, Drop Foot 		51 0 1 2.2E-03 0 0
CUI: C0441683
Disease: Hormone measurement
Hormone measurement 		51 0 1 2.2E-03 0 0
CUI: C2677180
Disease: Congenital microcephaly
Congenital microcephaly 		51 0 1 2.2E-03 0 0
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement 		50 0 1 2.2E-03 0 0
CUI: C1843700
Disease: Increased variability in muscle fiber diameter
Increased variability in muscle fiber diameter 		50 0 1 2.2E-03 0 0
CUI: C4317146
Disease: Acid reflux
Acid reflux 		50 0 1 2.2E-03 0 0
CUI: C0262361
Disease: Growth abnormality
Growth abnormality 		49 0 1 2.2E-03 0 0
CUI: C0265677
Disease: Congenital hemivertebra
Congenital hemivertebra 		49 0 1 2.2E-03 0 0
CUI: C1395852
Disease: Polydactyly preaxial type 1
Polydactyly preaxial type 1 		49 0 1 2.2E-03 0 0
CUI: C1857704
Disease: Abnormal myelination
Abnormal myelination 		49 0 1 2.2E-03 0 0
CUI: C0013069
Disease: Double Outlet Right Ventricle
Double Outlet Right Ventricle 		48 0 1 2.2E-03 0 0
CUI: C0023980
Disease: Longevity
Longevity 		48 0 1 2.2E-03 0 0
CUI: C0233844
Disease: Clumsiness
Clumsiness 		48 0 1 2.2E-03 0 0
CUI: C0270914
Disease: Hereditary Motor and Sensory-Neuropathy Type II
Hereditary Motor and Sensory-Neuropathy Type II 		48 0 1 2.2E-03 0 0
CUI: C0271385
Disease: Horizontal Nystagmus
Horizontal Nystagmus 		48 0 1 2.2E-03 0 0
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy 		48 0 1 2.2E-03 0 0