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: C0013882
Disease: Elephantiasis
Elephantiasis 		0 6 0 0 1 3.2E-02
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 3.8E-02
CUI: C0741585
Disease: BODY ACHE
BODY ACHE 		0 1 0 0 1 3.8E-02
CUI: C3890602
Disease: Bodily Pain
Bodily Pain 		0 4 0 0 1 3.4E-02
CUI: C0311394
Disease: Difficulty walking
Difficulty walking 		224 0 1 2.0E-03 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex 		201 0 1 2.0E-03 0 0
CUI: C1861324
Disease: Short philtrum
Short philtrum 		182 0 1 2.1E-03 0 0
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement 		169 0 1 2.2E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 0 1 2.2E-03 0 0
CUI: C1854494
Disease: Slow progression
Slow progression 		165 0 1 2.2E-03 0 0
CUI: C1836038
Disease: Poor head control
Poor head control 		162 0 1 2.2E-03 0 0
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity 		147 0 1 2.3E-03 0 0
CUI: C0231686
Disease: Gait, Unsteady
Gait, Unsteady 		143 0 1 2.3E-03 0 0
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		135 0 1 2.4E-03 0 0
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		131 0 1 2.4E-03 0 0
CUI: C1837397
Disease: Severe global developmental delay
Severe global developmental delay 		130 0 1 2.4E-03 0 0
CUI: C0266483
Disease: Pachygyria
Pachygyria 		129 0 1 2.4E-03 0 0
CUI: C1629609
Disease: Age at menopause
Age at menopause 		129 0 1 2.4E-03 0 0
CUI: C0030232
Disease: Pallor
Pallor 		124 0 1 2.4E-03 0 0
CUI: C0037773
Disease: Spastic Paraplegia, Hereditary
Spastic Paraplegia, Hereditary 		123 0 1 2.4E-03 0 0
CUI: C0039070
Disease: Syncope
Syncope 		119 0 1 2.5E-03 0 0
CUI: C0162701
Disease: Polysomnography
Polysomnography 		119 0 1 2.5E-03 0 0
CUI: C0427065
Disease: Distal muscle weakness
Distal muscle weakness 		117 0 1 2.5E-03 0 0
CUI: C3665386
Disease: Abnormal vision
Abnormal vision 		115 0 1 2.5E-03 0 0
CUI: C4021726
Disease: EMG: myopathic abnormalities
EMG: myopathic abnormalities 		115 0 1 2.5E-03 0 0