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: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		56 535 1 9.1E-04 2 3.0E-03
CUI: C0177804
Disease: Bone Mineral Density Test
Bone Mineral Density Test 		54 0 1 9.1E-04 0 0
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders 		54 0 1 9.1E-04 0 0
CUI: C1278049
Disease: Serum gamma-glutamyl transferase measurement
Serum gamma-glutamyl transferase measurement 		54 0 1 9.1E-04 0 0
CUI: C0337443
Disease: Sodium measurement
Sodium measurement 		53 0 1 9.1E-04 0 0
CUI: C1860816
Disease: Preauricular skin tag
Preauricular skin tag 		53 0 1 9.1E-04 0 0
CUI: C0001126
Disease: Renal tubular acidosis
Renal tubular acidosis 		52 0 1 9.1E-04 0 0
CUI: C0239067
Disease: Difficulty walking up stairs
Difficulty walking up stairs 		51 0 1 9.1E-04 0 0
CUI: C0426789
Disease: Short thorax
Short thorax 		51 0 1 9.1E-04 0 0
CUI: C0427149
Disease: Gait, Drop Foot
Gait, Drop Foot 		51 0 1 9.1E-04 0 0
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders 		50 0 1 9.2E-04 0 0
CUI: C0238395
Disease: Male Pseudohermaphroditism
Male Pseudohermaphroditism 		50 0 1 9.2E-04 0 0
CUI: C0262361
Disease: Growth abnormality
Growth abnormality 		49 0 1 9.2E-04 0 0
CUI: C2237660
Disease: exudative macular degeneration
exudative macular degeneration 		49 0 1 9.2E-04 0 0
CUI: C0018520
Disease: Halitosis
Halitosis 		48 0 1 9.2E-04 0 0
CUI: C0271385
Disease: Horizontal Nystagmus
Horizontal Nystagmus 		48 0 1 9.2E-04 0 0
CUI: C1136179
Disease: Hammer Toe
Hammer Toe 		46 0 1 9.2E-04 0 0
CUI: C1860493
Disease: Abnormality of the sternum
Abnormality of the sternum 		46 0 1 9.2E-04 0 0
CUI: C0497202
Disease: Abnormal ocular motility
Abnormal ocular motility 		45 0 1 9.2E-04 0 0
CUI: C2112129
Disease: Postaxial foot polydactyly
Postaxial foot polydactyly 		45 0 1 9.2E-04 0 0
CUI: C0240421
Disease: Progressive muscle weakness
Progressive muscle weakness 		44 0 1 9.2E-04 0 0
CUI: C0427055
Disease: Facial Paresis
Facial Paresis 		44 0 1 9.2E-04 0 0
CUI: C1854387
Disease: Type 1 muscle fiber predominance
Type 1 muscle fiber predominance 		44 0 1 9.2E-04 0 0
CUI: C2076600
Disease: Influenza due to Influenza A virus subtype H1N1
Influenza due to Influenza A virus subtype H1N1 		44 0 1 9.2E-04 0 0
CUI: C0085623
Disease: Akinesia
Akinesia 		43 0 1 9.2E-04 0 0