Source: INFERRED ×
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: C0856975
Disease: Autistic behavior
Autistic behavior 		228 76 201 0.14 22 3.9E-02
CUI: C0424503
Disease: Dysmorphic facies
Dysmorphic facies 		269 106 204 0.13 41 7.2E-02
CUI: C0221354
Disease: Frontal bossing
Frontal bossing 		320 22 210 0.13 6 1.2E-02
CUI: C1836830
Disease: Developmental regression
Developmental regression 		324 78 205 0.13 24 4.3E-02
CUI: C0221355
Disease: Macrocephaly
Macrocephaly 		304 0 202 0.13 0 0
CUI: C3665347
Disease: Visual Impairment
Visual Impairment 		420 0 215 0.13 0 0
CUI: C0019209
Disease: Hepatomegaly
Hepatomegaly 		472 30 215 0.13 2 3.8E-03
CUI: C1865014
Disease: Long philtrum
Long philtrum 		282 16 192 0.12 6 1.2E-02
CUI: C0026351
Disease: Moderate intellectual disability
Moderate intellectual disability 		223 93 185 0.12 12 2.0E-02
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		344 208 198 0.12 16 2.3E-02
CUI: C1848207
Disease: Poor speech
Poor speech 		208 9 183 0.12 1 1.9E-03
CUI: C1865017
Disease: Thin upper lip vermilion
Thin upper lip vermilion 		211 25 183 0.12 8 1.5E-02
CUI: C0423109
Disease: Upward slant of palpebral fissure
Upward slant of palpebral fissure 		216 16 182 0.12 7 1.4E-02
CUI: C0026106
Disease: Mild Mental Retardation
Mild Mental Retardation 		269 48 186 0.12 11 2.0E-02
CUI: C1850049
Disease: Clinodactyly of the 5th finger
Clinodactyly of the 5th finger 		284 39 187 0.12 16 3.0E-02
CUI: C0017168
Disease: Gastroesophageal reflux disease
Gastroesophageal reflux disease 		281 31 186 0.12 2 3.7E-03
CUI: C0848558
Disease: Hypospadias
Hypospadias 		266 26 182 0.12 1 1.9E-03
CUI: C0040822
Disease: Tremor
Tremor 		345 21 190 0.12 5 9.6E-03
CUI: C0013362
Disease: Dysarthria
Dysarthria 		470 42 199 0.12 8 1.5E-02
CUI: C0020255
Disease: Hydrocephalus
Hydrocephalus 		297 24 177 0.11 4 7.6E-03
CUI: C0016202
Disease: Flatfoot
Flatfoot 		282 38 175 0.11 12 2.3E-02
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy 		271 46 170 0.11 14 2.6E-02
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects 		250 43 164 0.11 9 1.7E-02
CUI: C0027092
Disease: Myopia
Myopia 		325 104 171 0.11 17 2.9E-02
CUI: C1843367
Disease: Poor school performance
Poor school performance 		211 411 160 0.11 110 0.14