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: C0234516
Disease: Speech dysfunction
Speech dysfunction
1 0 1 0.50 0 0
Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation
1 0 1 0.50 0 0
CUI: C0027438
Disease: Nasopharyngeal Diseases
Nasopharyngeal Diseases
2 0 1 0.33 0 0
CUI: C0282512
Disease: Landau-Kleffner Syndrome
Landau-Kleffner Syndrome
2 0 1 0.33 0 0
CUI: C1112263
Disease: Atypical benign partial epilepsy
Atypical benign partial epilepsy
2 0 1 0.33 0 0
CUI: C0233726
Disease: Aprosodia
Aprosodia
3 0 1 0.25 0 0
CUI: C0302527
Disease: Pathological personality NOS
Pathological personality NOS
3 0 1 0.25 0 0
CUI: C0751512
Disease: Dysglossia
Dysglossia
3 0 1 0.25 0 0
CUI: C0751513
Disease: Rhinolalia
Rhinolalia
3 0 1 0.25 0 0
CUI: C0751514
Disease: Verbal Fluency Disorders
Verbal Fluency Disorders
3 0 1 0.25 0 0
CUI: C4023478
Disease: EEG with focal sharp waves
EEG with focal sharp waves
3 0 1 0.25 0 0
CUI: C3495145
Disease: Dyslalia
Dyslalia
4 0 1 0.20 0 0
CUI: C4024906
Disease: Hemifacial seizures
Hemifacial seizures
4 0 1 0.20 0 0
CUI: C0017250
Disease: Psychosexual identity disorder
Psychosexual identity disorder
5 0 1 0.17 0 0
Continuous spike and waves during slow sleep
5 0 1 0.17 0 0
EEG with centrotemporal focal spike waves
5 0 1 0.17 0 0
Mental Retardation, X-Linked, Syndromic, Christianson Type
6 0 1 0.14 0 0
CUI: C4022855
Disease: Abnormal involuntary eye movements
Abnormal involuntary eye movements
6 0 1 0.14 0 0
EEG with generalized epileptiform discharges
6 0 1 0.14 0 0
Central Nervous System Viral Diseases
7 0 1 0.12 0 0
CUI: C1838027
Disease: Incomprehensible speech
Incomprehensible speech
7 0 1 0.12 0 0
EEG with irregular generalized spike and wave complexes
7 0 1 0.12 0 0
CUI: C0009090
Disease: Cluttering
Cluttering
8 0 1 0.11 0 0
CUI: C0600272
Disease: Morphine Abuse
Morphine Abuse
8 0 1 0.11 0 0
CUI: C4023014
Disease: Stereotypical hand wringing
Stereotypical hand wringing
8 0 1 0.11 0 0