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: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 5.6E-02
CUI: C0751007
Disease: Intracranial Atherosclerosis
Intracranial Atherosclerosis 		0 2 0 0 1 7.7E-02
CUI: C1837217
Disease: Cleft lip, isolated
Cleft lip, isolated 		0 2 0 0 1 7.7E-02
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		264 0 1 2.0E-03 0 0
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy 		187 0 1 2.4E-03 0 0
CUI: C1861324
Disease: Short philtrum
Short philtrum 		182 0 1 2.4E-03 0 0
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement 		169 0 1 2.5E-03 0 0
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		163 0 1 2.5E-03 0 0
CUI: C1836038
Disease: Poor head control
Poor head control 		162 0 1 2.5E-03 0 0
CUI: C0266551
Disease: Congenital coloboma of iris
Congenital coloboma of iris 		148 0 1 2.6E-03 0 0
CUI: C4551485
Disease: Clinodactyly
Clinodactyly 		148 0 1 2.6E-03 0 0
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity 		147 0 1 2.6E-03 0 0
CUI: C0023264
Disease: Leigh Disease
Leigh Disease 		144 0 1 2.6E-03 0 0
CUI: C0037772
Disease: Spastic Paraplegia
Spastic Paraplegia 		144 0 1 2.6E-03 0 0
CUI: C0020490
Disease: Hyperopia
Hyperopia 		142 0 1 2.6E-03 0 0
CUI: C0005938
Disease: Bone Density
Bone Density 		138 0 1 2.7E-03 0 0
CUI: C0158731
Disease: Congenital pectus carinatum
Congenital pectus carinatum 		138 0 1 2.7E-03 0 0
CUI: C3828530
Disease: Platelet Component Distribution Width Measurement
Platelet Component Distribution Width Measurement 		134 0 1 2.7E-03 0 0
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		131 0 1 2.7E-03 0 0
CUI: C0079924
Disease: Oligohydramnios
Oligohydramnios 		129 0 1 2.7E-03 0 0
CUI: C0266483
Disease: Pachygyria
Pachygyria 		129 0 1 2.7E-03 0 0
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		124 0 1 2.8E-03 0 0
CUI: C0037773
Disease: Spastic Paraplegia, Hereditary
Spastic Paraplegia, Hereditary 		123 0 1 2.8E-03 0 0
CUI: C0013222
Disease: Drug Use Disorders
Drug Use Disorders 		121 0 1 2.8E-03 0 0
CUI: C0014877
Disease: Esotropia
Esotropia 		121 0 1 2.8E-03 0 0