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: C0036572
Disease: Seizures
Seizures 		2152 553 97 4.4E-02 6 1.1E-02
CUI: C1843367
Disease: Poor school performance
Poor school performance 		211 411 21 6.3E-02 6 1.4E-02
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding) 		160 246 16 5.6E-02 6 2.4E-02
CUI: C0013362
Disease: Dysarthria
Dysarthria 		487 54 57 9.9E-02 5 7.9E-02
CUI: C0028738
Disease: Nystagmus
Nystagmus 		833 95 70 7.7E-02 5 4.8E-02
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		967 579 53 5.0E-02 4 6.8E-03
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity 		580 48 78 0.12 4 6.9E-02
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		1825 553 103 5.5E-02 4 7.1E-03
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior 		176 22 16 5.3E-02 3 9.1E-02
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		1112 395 54 4.5E-02 3 7.4E-03
CUI: C0018681
Disease: Headache
Headache 		338 75 6 1.3E-02 3 3.5E-02
CUI: C0234979
Disease: Dysdiadochokinesis
Dysdiadochokinesis 		49 7 11 6.1E-02 3 0.17
CUI: C0549629
Disease: Abnormal delivery
Abnormal delivery 		32 37 5 2.9E-02 3 6.2E-02
CUI: C0575081
Disease: Gait abnormality
Gait abnormality 		312 23 17 3.9E-02 3 8.8E-02
CUI: C0751837
Disease: Gait Ataxia
Gait Ataxia 		172 17 31 0.11 3 0.11
CUI: C1384666
Disease: hearing impairment
hearing impairment 		740 337 21 2.4E-02 3 8.6E-03
CUI: C1842366
Disease: Low anterior hairline
Low anterior hairline 		71 17 8 3.9E-02 3 0.11
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia 		955 164 92 9.1E-02 3 1.7E-02
CUI: C4072903
Disease: Primary Caesarian section
Primary Caesarian section 		11 15 3 2.0E-02 3 0.12
CUI: C0014877
Disease: Esotropia
Esotropia 		121 39 5 1.9E-02 2 3.9E-02
CUI: C0020295
Disease: Hydronephrosis
Hydronephrosis 		253 18 7 1.8E-02 2 6.7E-02
CUI: C0024433
Disease: Macrostomia
Macrostomia 		148 11 7 2.5E-02 2 8.7E-02
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		362 247 33 7.0E-02 2 7.7E-03
CUI: C0029131
Disease: Abnormality of the optic nerve
Abnormality of the optic nerve 		18 11 2 1.3E-02 2 8.7E-02
CUI: C0037771
Disease: Paraparesis, Spastic
Paraparesis, Spastic 		75 37 13 6.3E-02 2 4.1E-02