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: C0028643
Disease: Numbness
Numbness 		0 2 0 0 1 6.2E-02
CUI: C0494491
Disease: Mononeuropathies
Mononeuropathies 		0 2 0 0 1 6.2E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		433 0 1 1.5E-03 0 0
CUI: C1854882
Disease: Absent speech
Absent speech 		232 0 1 2.1E-03 0 0
CUI: C1848207
Disease: Poor speech
Poor speech 		208 0 1 2.2E-03 0 0
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement 		169 0 1 2.4E-03 0 0
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate 		169 0 1 2.4E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 0 1 2.4E-03 0 0
CUI: C1854494
Disease: Slow progression
Slow progression 		165 0 1 2.4E-03 0 0
CUI: C1836038
Disease: Poor head control
Poor head control 		162 0 1 2.4E-03 0 0
CUI: C0020796
Disease: Profound Mental Retardation
Profound Mental Retardation 		160 0 1 2.4E-03 0 0
CUI: C1855285
Disease: Protruding ear
Protruding ear 		152 0 1 2.5E-03 0 0
CUI: C0917816
Disease: Mental deficiency
Mental deficiency 		148 0 1 2.5E-03 0 0
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity 		147 0 1 2.5E-03 0 0
CUI: C0023264
Disease: Leigh Disease
Leigh Disease 		144 0 1 2.5E-03 0 0
CUI: C0037772
Disease: Spastic Paraplegia
Spastic Paraplegia 		144 0 1 2.5E-03 0 0
CUI: C0025363
Disease: Mental Retardation, Psychosocial
Mental Retardation, Psychosocial 		142 0 1 2.5E-03 0 0
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		139 0 1 2.6E-03 0 0
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		139 0 1 2.6E-03 0 0
CUI: C3828530
Disease: Platelet Component Distribution Width Measurement
Platelet Component Distribution Width Measurement 		134 0 1 2.6E-03 0 0
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		131 0 1 2.6E-03 0 0
CUI: C0018498
Disease: Hair Color
Hair Color 		130 0 1 2.6E-03 0 0
CUI: C1837397
Disease: Severe global developmental delay
Severe global developmental delay 		130 0 1 2.6E-03 0 0
CUI: C0266483
Disease: Pachygyria
Pachygyria 		129 0 1 2.6E-03 0 0
CUI: C1629609
Disease: Age at menopause
Age at menopause 		129 0 1 2.6E-03 0 0