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: C1842564
Disease: Temporal epilepsy, familial
Temporal epilepsy, familial 		2 0 2 0.25 0 0
CUI: C4049182
Disease: Idiopathic partial epilepsy
Idiopathic partial epilepsy 		2 0 2 0.25 0 0
CUI: C4478700
Disease: Focal cortical dysplasia type IIa
Focal cortical dysplasia type IIa 		2 0 2 0.25 0 0
CUI: C1838062
Disease: Autosomal Dominant Lateral Temporal Lobe Epilepsy
Autosomal Dominant Lateral Temporal Lobe Epilepsy 		8 0 2 0.14 0 0
CUI: C0085541
Disease: Epilepsy, Frontal Lobe
Epilepsy, Frontal Lobe 		10 0 2 0.12 0 0
CUI: C0234461
Disease: aphasic
aphasic 		1 0 1 0.12 0 0
CUI: C0454578
Disease: Receptive aphasia (finding)
Receptive aphasia (finding) 		1 0 1 0.12 0 0
CUI: C1838049
Disease: Epilepsy, Nocturnal Frontal Lobe, Type 1
Epilepsy, Nocturnal Frontal Lobe, Type 1 		1 0 1 0.12 0 0
CUI: C4310708
Disease: EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 3
EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 3 		1 0 1 0.12 0 0
CUI: C4551983
Disease: EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 1
EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 1 		1 67 1 0.12 14 0.18
CUI: C0751112
Disease: Subclinical Seizure
Subclinical Seizure 		2 0 1 0.11 0 0
CUI: C1854335
Disease: Epilepsy, Nocturnal Frontal Lobe, Type 3
Epilepsy, Nocturnal Frontal Lobe, Type 3 		2 0 1 0.11 0 0
CUI: C1968848
Disease: Epilepsy, Familial Mesial Temporal Lobe
Epilepsy, Familial Mesial Temporal Lobe 		2 0 1 0.11 0 0
CUI: C0265482
Disease: Ring Chromosome 20 Syndrome
Ring Chromosome 20 Syndrome 		3 0 1 1.0E-01 0 0
CUI: C1835905
Disease: Epilepsy, Nocturnal Frontal Lobe, Type 4
Epilepsy, Nocturnal Frontal Lobe, Type 4 		3 0 1 1.0E-01 0 0
CUI: C1838063
Disease: Focal sensory auditory seizure
Focal sensory auditory seizure 		3 0 1 1.0E-01 0 0
CUI: C2930824
Disease: Autoimmune limbic encephalitis
Autoimmune limbic encephalitis 		3 0 1 1.0E-01 0 0
CUI: C4310709
Disease: EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 2
EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 2 		3 0 1 1.0E-01 0 0
CUI: C4706583
Disease: Limbic encephalitis with leucine-rich glioma-inactivated 1 antibodies
Limbic encephalitis with leucine-rich glioma-inactivated 1 antibodies 		3 0 1 1.0E-01 0 0
CUI: C0234974
Disease: Simple Partial Seizures
Simple Partial Seizures 		4 0 1 9.1E-02 0 0
CUI: C0391958
Disease: Familial Epilepsies
Familial Epilepsies 		16 0 2 9.1E-02 0 0
CUI: C0393671
Disease: Frontal Epilepsy, Benign, Childhood
Frontal Epilepsy, Benign, Childhood 		4 0 1 9.1E-02 0 0
CUI: C0393683
Disease: Epilepsy, Supplementary Motor
Epilepsy, Supplementary Motor 		4 0 1 9.1E-02 0 0
CUI: C0393684
Disease: Epilepsy, Cingulate
Epilepsy, Cingulate 		4 0 1 9.1E-02 0 0
CUI: C0393688
Disease: Epilepsy, Opercular
Epilepsy, Opercular 		4 0 1 9.1E-02 0 0