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: C0278061
Disease: Abnormal mental state
Abnormal mental state
24 0 16 0.21 0 0
CUI: C1306341
Disease: Mental handicap
Mental handicap
26 0 16 0.21 0 0
CUI: C0262405
Disease: Cerebral dysfunction
Cerebral dysfunction
45 0 8 7.7E-02 0 0
CUI: C0086237
Disease: Epilepsy, Cryptogenic
Epilepsy, Cryptogenic
88 0 11 7.6E-02 0 0
CUI: C0236018
Disease: Aura
Aura
83 0 10 7.1E-02 0 0
CUI: C0751111
Disease: Awakening Epilepsy
Awakening Epilepsy
83 0 10 7.1E-02 0 0
Malformations of Cortical Development
60 0 8 6.7E-02 0 0
CUI: C0025362
Disease: Mental Retardation
Mental Retardation
505 0 36 6.7E-02 0 0
CUI: C0162635
Disease: Angelman Syndrome
Angelman Syndrome
94 0 10 6.6E-02 0 0
CUI: C0240379
Disease: Open mouth (finding)
Open mouth (finding)
96 11 10 6.5E-02 1 4.2E-02
CUI: C1843367
Disease: Poor school performance
Poor school performance
211 411 17 6.5E-02 2 4.7E-03
CUI: C0042024
Disease: Urinary Incontinence
Urinary Incontinence
151 0 13 6.3E-02 0 0
CUI: C0751265
Disease: Learning Disabilities
Learning Disabilities
103 0 10 6.2E-02 0 0
CUI: C0020796
Disease: Profound Mental Retardation
Profound Mental Retardation
160 0 13 6.1E-02 0 0
CUI: C0085271
Disease: Self-Injurious Behavior
Self-Injurious Behavior
91 0 9 6.0E-02 0 0
CUI: C1858036
Disease: Periorbital fullness
Periorbital fullness
57 0 7 6.0E-02 0 0
CUI: C2315100
Disease: Pediatric failure to thrive
Pediatric failure to thrive
166 0 13 5.9E-02 0 0
CUI: C0038271
Disease: Stereotyped Behavior
Stereotyped Behavior
135 0 11 5.8E-02 0 0
CUI: C0036857
Disease: Severe intellectual disability
Severe intellectual disability
429 0 27 5.8E-02 0 0
CUI: C0026351
Disease: Moderate intellectual disability
Moderate intellectual disability
251 0 17 5.6E-02 0 0
CUI: C0751156
Disease: FRAXA Syndrome
FRAXA Syndrome
8 0 4 5.6E-02 0 0
CUI: C1136249
Disease: Mental Retardation, X-Linked
Mental Retardation, X-Linked
141 0 11 5.6E-02 0 0
CUI: C0917816
Disease: Mental deficiency
Mental deficiency
148 0 11 5.4E-02 0 0
CUI: C1862389
Disease: ATRIAL SEPTAL DEFECT 1
ATRIAL SEPTAL DEFECT 1
91 0 8 5.3E-02 0 0
CUI: C0549629
Disease: Abnormal delivery
Abnormal delivery
32 0 5 5.3E-02 0 0