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: C0005938
Disease: Bone Density
Bone Density 		138 0 1 3.6E-03 0 0
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		138 0 1 3.6E-03 0 0
CUI: C4048268
Disease: Cortical visual impairment
Cortical visual impairment 		136 0 1 3.6E-03 0 0
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		131 0 1 3.6E-03 0 0
CUI: C0018498
Disease: Hair Color
Hair Color 		130 0 1 3.7E-03 0 0
CUI: C0024636
Disease: Malocclusion
Malocclusion 		128 0 1 3.7E-03 0 0
CUI: C1328407
Disease: Hip Dysplasia
Hip Dysplasia 		128 0 1 3.7E-03 0 0
CUI: C0014877
Disease: Esotropia
Esotropia 		121 0 1 3.8E-03 0 0
CUI: C0021704
Disease: Intelligence
Intelligence 		645 0 3 3.8E-03 0 0
CUI: C0162701
Disease: Polysomnography
Polysomnography 		119 0 1 3.8E-03 0 0
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle 		118 0 1 3.8E-03 0 0
CUI: C1837658
Disease: Gross motor development delay
Gross motor development delay 		118 0 1 3.8E-03 0 0
CUI: C4552811
Disease: Generalized Muscle Weakness, CTCAE
Generalized Muscle Weakness, CTCAE 		117 0 1 3.8E-03 0 0
CUI: C1839758
Disease: Narrow forehead
Narrow forehead 		106 0 1 4.0E-03 0 0
CUI: C0342276
Disease: Maturity onset diabetes mellitus in young
Maturity onset diabetes mellitus in young 		105 0 1 4.0E-03 0 0
CUI: C1142533
Disease: Smooth philtrum
Smooth philtrum 		105 0 1 4.0E-03 0 0
CUI: C0175702
Disease: Williams Syndrome
Williams Syndrome 		104 0 1 4.0E-03 0 0
CUI: C0600260
Disease: Lung Diseases, Obstructive
Lung Diseases, Obstructive 		104 0 1 4.0E-03 0 0
CUI: C1837142
Disease: Poor suck
Poor suck 		103 0 1 4.1E-03 0 0
CUI: C0003706
Disease: Arachnodactyly
Arachnodactyly 		102 0 1 4.1E-03 0 0
CUI: C4021786
Disease: Atypical scarring of skin
Atypical scarring of skin 		101 0 1 4.1E-03 0 0
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		100 0 1 4.1E-03 0 0
CUI: C0917796
Disease: Optic Atrophy, Hereditary, Leber
Optic Atrophy, Hereditary, Leber 		100 0 1 4.1E-03 0 0
CUI: C0546126
Disease: Acute Confusional Senile Dementia
Acute Confusional Senile Dementia 		99 0 1 4.1E-03 0 0
CUI: C0750900
Disease: Alzheimer's Disease, Focal Onset
Alzheimer's Disease, Focal Onset 		99 0 1 4.1E-03 0 0