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: C4024906
Disease: Hemifacial seizures
Hemifacial seizures 		4 0 4 0.57 0 0
CUI: C4022848
Disease: EEG with centrotemporal focal spike waves
EEG with centrotemporal focal spike waves 		5 0 3 0.33 0 0
CUI: C3552824
Disease: Enhancement of the C-reflex
Enhancement of the C-reflex 		2 0 2 0.29 0 0
CUI: C3552825
Disease: Jerk-locked premyoclonus spikes
Jerk-locked premyoclonus spikes 		2 0 2 0.29 0 0
CUI: C3552821
Disease: EEG with photoparoxysmal response
EEG with photoparoxysmal response 		3 0 2 0.25 0 0
CUI: C4023478
Disease: EEG with focal sharp waves
EEG with focal sharp waves 		3 0 2 0.25 0 0
CUI: C1832841
Disease: EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1
EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1 		4 0 2 0.22 0 0
CUI: C3806961
Disease: Giant somatosensory evoked potentials
Giant somatosensory evoked potentials 		4 0 2 0.22 0 0
CUI: C0917800
Disease: Epilepsy, Myoclonic, Infantile
Epilepsy, Myoclonic, Infantile 		11 0 3 0.20 0 0
CUI: C3806403
Disease: Continuous spike and waves during slow sleep
Continuous spike and waves during slow sleep 		5 0 2 0.20 0 0
CUI: C4023476
Disease: EEG with generalized epileptiform discharges
EEG with generalized epileptiform discharges 		6 0 2 0.18 0 0
CUI: C1838027
Disease: Incomprehensible speech
Incomprehensible speech 		7 0 2 0.17 0 0
CUI: C2363129
Disease: Benign Rolandic Epilepsy
Benign Rolandic Epilepsy 		15 0 3 0.16 0 0
CUI: C0006009
Disease: Borderline intellectual disability
Borderline intellectual disability 		16 0 3 0.15 0 0
CUI: C0234516
Disease: Speech dysfunction
Speech dysfunction 		1 0 1 0.14 0 0
CUI: C0595948
Disease: Atypical absence seizure
Atypical absence seizure 		17 0 3 0.14 0 0
CUI: C0795927
Disease: Deafness, congenital onychodystrophy, recessive form
Deafness, congenital onychodystrophy, recessive form 		1 0 1 0.14 0 0
CUI: C1842531
Disease: Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp
Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp 		1 0 1 0.14 0 0
CUI: C1843244
Disease: EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2 		1 0 1 0.14 0 0
CUI: C1845070
Disease: Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked
Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked 		1 0 1 0.14 0 0
CUI: C1858674
Disease: GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3 		1 0 1 0.14 0 0
CUI: C2829265
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 86
DEAFNESS, AUTOSOMAL RECESSIVE 86 		1 0 1 0.14 0 0
CUI: C3809173
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16 		1 0 1 0.14 0 0
CUI: C3809181
Disease: Caused by mutation in the TBC1 domain family, member 24 gene (TBC1D24, 613577.0004)
Caused by mutation in the TBC1 domain family, member 24 gene (TBC1D24, 613577.0004) 		1 0 1 0.14 0 0
CUI: C3892048
Disease: DEAFNESS, AUTOSOMAL DOMINANT 65
DEAFNESS, AUTOSOMAL DOMINANT 65 		1 0 1 0.14 0 0