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: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 1.8E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 2.0E-02
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 1 2.0E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 2.0E-02
CUI: C0034935
Disease: Babinski Reflex
Babinski Reflex 		218 0 1 2.0E-03 0 0
CUI: C1848207
Disease: Poor speech
Poor speech 		208 0 1 2.0E-03 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex 		201 0 1 2.0E-03 0 0
CUI: C0266464
Disease: Polymicrogyria
Polymicrogyria 		199 0 1 2.0E-03 0 0
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement 		169 0 1 2.2E-03 0 0
CUI: C1854494
Disease: Slow progression
Slow progression 		165 0 1 2.2E-03 0 0
CUI: C0265610
Disease: Clinodactyly of fingers
Clinodactyly of fingers 		160 0 1 2.2E-03 0 0
CUI: C1853743
Disease: Muscular hypotonia of the trunk
Muscular hypotonia of the trunk 		156 0 1 2.2E-03 0 0
CUI: C0684276
Disease: Hypsarrhythmia
Hypsarrhythmia 		152 0 1 2.2E-03 0 0
CUI: C0266551
Disease: Congenital coloboma of iris
Congenital coloboma of iris 		148 0 1 2.3E-03 0 0
CUI: C0917816
Disease: Mental deficiency
Mental deficiency 		148 0 1 2.3E-03 0 0
CUI: C4551485
Disease: Clinodactyly
Clinodactyly 		148 0 1 2.3E-03 0 0
CUI: C1858430
Disease: Death in infancy
Death in infancy 		146 0 1 2.3E-03 0 0
CUI: C1839739
Disease: Thick lower lip vermilion
Thick lower lip vermilion 		145 0 1 2.3E-03 0 0
CUI: C0037772
Disease: Spastic Paraplegia
Spastic Paraplegia 		144 0 1 2.3E-03 0 0
CUI: C0231686
Disease: Gait, Unsteady
Gait, Unsteady 		143 0 1 2.3E-03 0 0
CUI: C0020490
Disease: Hyperopia
Hyperopia 		142 0 1 2.3E-03 0 0
CUI: C0025363
Disease: Mental Retardation, Psychosocial
Mental Retardation, Psychosocial 		142 0 1 2.3E-03 0 0
CUI: C4048268
Disease: Cortical visual impairment
Cortical visual impairment 		136 0 1 2.3E-03 0 0
CUI: C0038271
Disease: Stereotyped Behavior
Stereotyped Behavior 		135 0 1 2.3E-03 0 0
CUI: C0018498
Disease: Hair Color
Hair Color 		130 0 1 2.4E-03 0 0