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 1 1.1E-03 0 0
CUI: C1305855
Disease: Body mass index
Body mass index 		1014 0 2 1.8E-03 0 0
CUI: C0042834
Disease: Vital capacity
Vital capacity 		430 0 1 2.0E-03 0 0
CUI: C0021704
Disease: Intelligence
Intelligence 		645 0 2 2.8E-03 0 0
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		578 0 2 3.0E-03 0 0
CUI: C1854882
Disease: Absent speech
Absent speech 		232 0 1 3.2E-03 0 0
CUI: C0235480
Disease: Paroxysmal atrial fibrillation
Paroxysmal atrial fibrillation 		226 0 1 3.3E-03 0 0
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies 		219 0 1 3.4E-03 0 0
CUI: C0001125
Disease: Acidosis, Lactic
Acidosis, Lactic 		209 0 1 3.5E-03 0 0
CUI: C1848207
Disease: Poor speech
Poor speech 		208 0 1 3.5E-03 0 0
CUI: C0040420
Disease: Tonometry
Tonometry 		206 0 1 3.5E-03 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex 		201 0 1 3.6E-03 0 0
CUI: C0240066
Disease: Iron deficiency
Iron deficiency 		179 0 1 3.9E-03 0 0
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		433 0 2 3.9E-03 0 0
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement 		169 0 1 4.0E-03 0 0
CUI: C0403823
Disease: Asthenozoospermia
Asthenozoospermia 		164 0 1 4.1E-03 0 0
CUI: C1862939
Disease: AMYOTROPHIC LATERAL SCLEROSIS 1
AMYOTROPHIC LATERAL SCLEROSIS 1 		164 0 1 4.1E-03 0 0
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		163 0 1 4.1E-03 0 0
CUI: C0023380
Disease: Lethargy
Lethargy 		160 0 1 4.2E-03 0 0
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		399 0 2 4.2E-03 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		158 0 1 4.2E-03 0 0
CUI: C0038580
Disease: Substance Dependence
Substance Dependence 		156 0 1 4.3E-03 0 0
CUI: C0087012
Disease: Ataxia, Spinocerebellar
Ataxia, Spinocerebellar 		156 0 1 4.3E-03 0 0
CUI: C1853743
Disease: Muscular hypotonia of the trunk
Muscular hypotonia of the trunk 		156 0 1 4.3E-03 0 0
CUI: C0022735
Disease: Klinefelter Syndrome
Klinefelter Syndrome 		150 0 1 4.4E-03 0 0