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: C1836830
Disease: Developmental regression
Developmental regression 		333 0 1 2.1E-03 0 0
CUI: C0221354
Disease: Frontal bossing
Frontal bossing 		321 0 1 2.1E-03 0 0
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		272 0 1 2.4E-03 0 0
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		269 0 1 2.4E-03 0 0
CUI: C1314691
Disease: Age at menarche
Age at menarche 		267 0 1 2.4E-03 0 0
CUI: C0856975
Disease: Autistic behavior
Autistic behavior 		261 0 1 2.4E-03 0 0
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		249 0 1 2.5E-03 0 0
CUI: C0266435
Disease: Congenital hypoplasia of penis
Congenital hypoplasia of penis 		237 0 1 2.6E-03 0 0
CUI: C1853242
Disease: Midface retrusion
Midface retrusion 		228 0 1 2.6E-03 0 0
CUI: C0151611
Disease: Electroencephalogram abnormal
Electroencephalogram abnormal 		227 0 1 2.6E-03 0 0
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		223 0 1 2.7E-03 0 0
CUI: C0020608
Disease: Hypodontia
Hypodontia 		218 0 1 2.7E-03 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		215 0 1 2.7E-03 0 0
CUI: C1843367
Disease: Poor school performance
Poor school performance 		211 0 1 2.7E-03 0 0
CUI: C1848207
Disease: Poor speech
Poor speech 		208 0 1 2.8E-03 0 0
CUI: C0410528
Disease: Skeletal dysplasia
Skeletal dysplasia 		186 0 1 2.9E-03 0 0
CUI: C0037822
Disease: Speech Disorders
Speech Disorders 		183 0 1 3.0E-03 0 0
CUI: C0596887
Disease: mathematical ability
mathematical ability 		854 0 3 3.0E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior 		176 0 1 3.0E-03 0 0
CUI: C0423224
Disease: Sunken eyes
Sunken eyes 		171 0 1 3.1E-03 0 0
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate 		169 0 1 3.1E-03 0 0
CUI: C0020796
Disease: Profound Mental Retardation
Profound Mental Retardation 		160 0 1 3.2E-03 0 0
CUI: C1837260
Disease: Prominent forehead
Prominent forehead 		159 0 1 3.2E-03 0 0
CUI: C0234132
Disease: Pyramidal sign
Pyramidal sign 		155 0 1 3.2E-03 0 0
CUI: C0221358
Disease: Long narrow head
Long narrow head 		154 0 1 3.3E-03 0 0