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: C1112263
Disease: Atypical benign partial epilepsy
Atypical benign partial epilepsy 		2 0 2 1.00 0 0
CUI: C0234516
Disease: Speech dysfunction
Speech dysfunction 		1 0 1 0.50 0 0
CUI: C3472470
Disease: Severe major depression
Severe major depression 		1 0 1 0.50 0 0
CUI: C3714689
Disease: Obsessional personality disorder
Obsessional personality disorder 		1 0 1 0.50 0 0
CUI: C4749281
Disease: Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation
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: C0236816
Disease: Stress Disorders, Traumatic, Acute
Stress Disorders, Traumatic, Acute 		2 0 1 0.33 0 0
CUI: C3806402
Disease: EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION
EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION 		2 0 1 0.33 0 0
CUI: C0020604
Disease: Hypochondriasis
Hypochondriasis 		3 0 1 0.25 0 0
CUI: C0233726
Disease: Aprosodia
Aprosodia 		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: C4050504
Disease: Ectomesenchymal Chondromyxoid Tumor
Ectomesenchymal Chondromyxoid Tumor 		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: C3806403
Disease: Continuous spike and waves during slow sleep
Continuous spike and waves during slow sleep 		5 0 1 0.17 0 0
CUI: C4022848
Disease: EEG with centrotemporal focal spike waves
EEG with centrotemporal focal spike waves 		5 0 1 0.17 0 0
CUI: C2678194
Disease: Mental Retardation, X-Linked, Syndromic, Christianson Type
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
CUI: C4023476
Disease: EEG with generalized epileptiform discharges
EEG with generalized epileptiform discharges 		6 0 1 0.14 0 0
CUI: C2363129
Disease: Benign Rolandic Epilepsy
Benign Rolandic Epilepsy 		15 0 2 0.13 0 0
CUI: C0348165
Disease: Central Nervous System Viral Diseases
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