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: C0221356
Disease: Brachycephaly
Brachycephaly 		186 0 1 2.7E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior 		176 0 1 2.7E-03 0 0
CUI: C0431478
Disease: Posteriorly rotated ear
Posteriorly rotated ear 		176 0 1 2.7E-03 0 0
CUI: C0026034
Disease: Microstomia
Microstomia 		172 0 1 2.8E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 0 1 2.8E-03 0 0
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		166 0 1 2.8E-03 0 0
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		166 0 1 2.8E-03 0 0
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		166 0 1 2.8E-03 0 0
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		165 0 1 2.8E-03 0 0
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		163 0 1 2.8E-03 0 0
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding) 		160 0 1 2.9E-03 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		158 0 1 2.9E-03 0 0
CUI: C0684276
Disease: Hypsarrhythmia
Hypsarrhythmia 		152 0 1 2.9E-03 0 0
CUI: C1855285
Disease: Protruding ear
Protruding ear 		152 0 1 2.9E-03 0 0
CUI: C0024433
Disease: Macrostomia
Macrostomia 		148 0 1 3.0E-03 0 0
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		146 0 1 3.0E-03 0 0
CUI: C1868571
Disease: Highly arched eyebrow
Highly arched eyebrow 		141 0 1 3.0E-03 0 0
CUI: C0005938
Disease: Bone Density
Bone Density 		138 0 1 3.1E-03 0 0
CUI: C0010964
Disease: Dandy-Walker Syndrome
Dandy-Walker Syndrome 		137 0 1 3.1E-03 0 0
CUI: C0266589
Disease: Congenital ear anomaly NOS (disorder)
Congenital ear anomaly NOS (disorder) 		137 0 1 3.1E-03 0 0
CUI: C4048268
Disease: Cortical visual impairment
Cortical visual impairment 		136 0 1 3.1E-03 0 0
CUI: C0009363
Disease: Congenital ocular coloboma (disorder)
Congenital ocular coloboma (disorder) 		129 0 1 3.1E-03 0 0
CUI: C0266483
Disease: Pachygyria
Pachygyria 		129 0 1 3.1E-03 0 0
CUI: C0266544
Disease: Microcornea
Microcornea 		129 0 1 3.1E-03 0 0
CUI: C1848673
Disease: Hypoplastic feet
Hypoplastic feet 		129 0 1 3.1E-03 0 0