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: C4551957
Disease: Epilepsy, Familial Temporal Lobe 1
Epilepsy, Familial Temporal Lobe 1 		7 17 6 0.67 2 0.11
CUI: C1842564
Disease: Temporal epilepsy, familial
Temporal epilepsy, familial 		2 0 2 0.25 0 0
CUI: C1838063
Disease: Focal sensory auditory seizure
Focal sensory auditory seizure 		3 0 2 0.22 0 0
CUI: C0234974
Disease: Simple Partial Seizures
Simple Partial Seizures 		4 0 2 0.20 0 0
CUI: C1858477
Disease: Epilepsy, Partial, with Variable Foci
Epilepsy, Partial, with Variable Foci 		8 0 2 0.14 0 0
CUI: C0234461
Disease: aphasic
aphasic 		1 0 1 0.12 0 0
CUI: C0406821
Disease: Rhabdomyomatous mesenchymal hamartoma
Rhabdomyomatous mesenchymal hamartoma 		1 0 1 0.12 0 0
CUI: C0454578
Disease: Receptive aphasia (finding)
Receptive aphasia (finding) 		1 1 1 0.12 1 0.25
CUI: C0796089
Disease: LISSENCEPHALY SYNDROME, NORMAN-ROBERTS TYPE
LISSENCEPHALY SYNDROME, NORMAN-ROBERTS TYPE 		1 0 1 0.12 0 0
CUI: C1274890
Disease: Midline cervical cleft
Midline cervical cleft 		1 0 1 0.12 0 0
CUI: C1862491
Disease: Internally rotated shoulders
Internally rotated shoulders 		1 0 1 0.12 0 0
CUI: C2959380
Disease: Folliculosebaceous cystic hamartoma
Folliculosebaceous cystic hamartoma 		1 0 1 0.12 0 0
CUI: C4225327
Disease: EPILEPSY, FAMILIAL TEMPORAL LOBE, 7
EPILEPSY, FAMILIAL TEMPORAL LOBE, 7 		1 0 1 0.12 0 0
CUI: C4479539
Disease: ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT
ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT 		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 0 1 0.12 0 0
CUI: C4693688
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 61
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 61 		1 0 1 0.12 0 0
CUI: C0751112
Disease: Subclinical Seizure
Subclinical Seizure 		2 0 1 0.11 0 0
CUI: C1858493
Disease: FEBRILE CONVULSIONS, FAMILIAL, 4
FEBRILE CONVULSIONS, FAMILIAL, 4 		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: C1969656
Disease: MYOCLONIC EPILEPSY, JUVENILE, SUSCEPTIBILITY TO, 4 (disorder)
MYOCLONIC EPILEPSY, JUVENILE, SUSCEPTIBILITY TO, 4 (disorder) 		2 0 1 0.11 0 0
CUI: C2676439
Disease: USHER SYNDROME, TYPE IIB, FORMERLY
USHER SYNDROME, TYPE IIB, FORMERLY 		2 0 1 0.11 0 0
CUI: C3148929
Disease: USHER SYNDROME, TYPE IIC, GPR98/PDZD7 DIGENIC
USHER SYNDROME, TYPE IIC, GPR98/PDZD7 DIGENIC 		2 0 1 0.11 0 0
CUI: C4025124
Disease: Limited elbow extension and supination
Limited elbow extension and supination 		2 0 1 0.11 0 0
CUI: C4049182
Disease: Idiopathic partial epilepsy
Idiopathic partial epilepsy 		2 0 1 0.11 0 0
CUI: C4478700
Disease: Focal cortical dysplasia type IIa
Focal cortical dysplasia type IIa 		2 0 1 0.11 0 0