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: C1301260
Disease: Gastrointestinal Crohn's disease
Gastrointestinal Crohn's disease 		0 2 0 0 1 0.12
CUI: C1853438
Disease: INFLAMMATORY BOWEL DISEASE 5
INFLAMMATORY BOWEL DISEASE 5 		0 2 0 0 1 0.12
CUI: C2363867
Disease: Bacterascites
Bacterascites 		0 2 0 0 1 0.12
CUI: C4310747
Disease: CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 5
CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 5 		0 2 0 0 1 0.12
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		578 0 2 2.6E-03 0 0
CUI: C1836038
Disease: Poor head control
Poor head control 		162 0 1 2.8E-03 0 0
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		160 0 1 2.8E-03 0 0
CUI: C3468561
Disease: familial atrial fibrillation
familial atrial fibrillation 		157 0 1 2.8E-03 0 0
CUI: C2585653
Disease: Persistent atrial fibrillation
Persistent atrial fibrillation 		156 0 1 2.8E-03 0 0
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		146 0 1 2.9E-03 0 0
CUI: C0009171
Disease: Cocaine Abuse
Cocaine Abuse 		144 0 1 2.9E-03 0 0
CUI: C0037772
Disease: Spastic Paraplegia
Spastic Paraplegia 		144 0 1 2.9E-03 0 0
CUI: C0020490
Disease: Hyperopia
Hyperopia 		142 0 1 2.9E-03 0 0
CUI: C0005938
Disease: Bone Density
Bone Density 		138 0 1 3.0E-03 0 0
CUI: C0393525
Disease: Progressive cerebellar ataxia
Progressive cerebellar ataxia 		136 0 1 3.0E-03 0 0
CUI: C4048268
Disease: Cortical visual impairment
Cortical visual impairment 		136 0 1 3.0E-03 0 0
CUI: C0018498
Disease: Hair Color
Hair Color 		130 0 1 3.1E-03 0 0
CUI: C1629609
Disease: Age at menopause
Age at menopause 		129 0 1 3.1E-03 0 0
CUI: C0234162
Disease: Cerebellar Dysmetria
Cerebellar Dysmetria 		127 0 1 3.1E-03 0 0
CUI: C0746674
Disease: Generalized muscle weakness
Generalized muscle weakness 		126 0 1 3.1E-03 0 0
CUI: C0240543
Disease: Bulbous nose
Bulbous nose 		123 0 1 3.1E-03 0 0
CUI: C0025521
Disease: Inborn Errors of Metabolism
Inborn Errors of Metabolism 		119 0 1 3.2E-03 0 0
CUI: C0162701
Disease: Polysomnography
Polysomnography 		119 0 1 3.2E-03 0 0
CUI: C1837658
Disease: Gross motor development delay
Gross motor development delay 		118 0 1 3.2E-03 0 0
CUI: C1860834
Disease: Infantile muscular hypotonia
Infantile muscular hypotonia 		118 0 1 3.2E-03 0 0