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: C0021704
Disease: Intelligence
Intelligence 		645 0 1 1.2E-03 0 0
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies 		219 0 1 2.3E-03 0 0
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement 		169 0 1 2.6E-03 0 0
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		168 0 1 2.6E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 0 1 2.6E-03 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		158 0 1 2.6E-03 0 0
CUI: C1853743
Disease: Muscular hypotonia of the trunk
Muscular hypotonia of the trunk 		156 0 1 2.7E-03 0 0
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity 		147 0 1 2.7E-03 0 0
CUI: C0231686
Disease: Gait, Unsteady
Gait, Unsteady 		143 0 1 2.8E-03 0 0
CUI: C0005938
Disease: Bone Density
Bone Density 		138 0 1 2.8E-03 0 0
CUI: C0018498
Disease: Hair Color
Hair Color 		130 0 1 2.9E-03 0 0
CUI: C1837397
Disease: Severe global developmental delay
Severe global developmental delay 		130 0 1 2.9E-03 0 0
CUI: C1629609
Disease: Age at menopause
Age at menopause 		129 0 1 2.9E-03 0 0
CUI: C1866195
Disease: Downturned corners of mouth
Downturned corners of mouth 		122 0 1 2.9E-03 0 0
CUI: C1866934
Disease: Reduced tendon reflexes
Reduced tendon reflexes 		121 0 1 2.9E-03 0 0
CUI: C0266362
Disease: Ambiguous Genitalia
Ambiguous Genitalia 		109 0 1 3.0E-03 0 0
CUI: C4021085
Disease: Abnormality of brain morphology
Abnormality of brain morphology 		104 0 1 3.1E-03 0 0
CUI: C4551493
Disease: Situs inversus totalis
Situs inversus totalis 		104 0 1 3.1E-03 0 0
CUI: C0270685
Disease: Cerebral calcification
Cerebral calcification 		103 0 1 3.1E-03 0 0
CUI: C0019337
Disease: Heroin Dependence
Heroin Dependence 		100 0 1 3.1E-03 0 0
CUI: C0015644
Disease: Muscular fasciculation
Muscular fasciculation 		99 0 1 3.1E-03 0 0
CUI: C0424230
Disease: Motor retardation
Motor retardation 		98 0 1 3.1E-03 0 0
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis 		95 0 1 3.2E-03 0 0
CUI: C0009398
Disease: Color vision defect
Color vision defect 		94 0 1 3.2E-03 0 0
CUI: C0020305
Disease: Hydrops Fetalis
Hydrops Fetalis 		92 0 1 3.2E-03 0 0