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: C4023499
Disease: Generalized clonic seizures
Generalized clonic seizures 		18 0 3 0.12 0 0
CUI: C1852581
Disease: EPILEPSY, BENIGN NEONATAL, 2
EPILEPSY, BENIGN NEONATAL, 2 		9 0 2 0.12 0 0
CUI: C3889476
Disease: Benign Familial Convulsion
Benign Familial Convulsion 		9 0 2 0.12 0 0
CUI: C0393703
Disease: Myoclonic Absence Epilepsy
Myoclonic Absence Epilepsy 		10 0 2 0.11 0 0
CUI: C0917800
Disease: Epilepsy, Myoclonic, Infantile
Epilepsy, Myoclonic, Infantile 		11 0 2 0.11 0 0
CUI: C0014122
Disease: Subacute Bacterial Endocarditis
Subacute Bacterial Endocarditis 		12 0 2 1.0E-01 0 0
CUI: C0393693
Disease: Benign Neonatal Epilepsy, Nonfamilial
Benign Neonatal Epilepsy, Nonfamilial 		1 0 1 1.0E-01 0 0
CUI: C1262106
Disease: Neuromuscular toxicity
Neuromuscular toxicity 		1 0 1 1.0E-01 0 0
CUI: C2677326
Disease: Epileptic Encephalopathy, Early Infantile, 4
Epileptic Encephalopathy, Early Infantile, 4 		1 0 1 1.0E-01 0 0
CUI: C2751195
Disease: Epilepsy, Benign Neonatal, 1, And-Or Myokymia
Epilepsy, Benign Neonatal, 1, And-Or Myokymia 		1 0 1 1.0E-01 0 0
CUI: C3149074
Disease: SEIZURES, BENIGN FAMILIAL NEONATAL, 1
SEIZURES, BENIGN FAMILIAL NEONATAL, 1 		1 0 1 1.0E-01 0 0
CUI: C3149075
Disease: SEIZURES, BENIGN FAMILIAL NEONATAL, 1, AND/OR MYOKYMIA
SEIZURES, BENIGN FAMILIAL NEONATAL, 1, AND/OR MYOKYMIA 		1 0 1 1.0E-01 0 0
CUI: C3150731
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5 		1 0 1 1.0E-01 0 0
CUI: C3150986
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7 		1 0 1 1.0E-01 0 0
CUI: C3264000
Disease: Refractory juvenile myoclonic epilepsy
Refractory juvenile myoclonic epilepsy 		1 0 1 1.0E-01 0 0
CUI: C3275508
Disease: MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2
MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2 		1 0 1 1.0E-01 0 0
CUI: C3541908
Disease: Sperm Motility Measurement
Sperm Motility Measurement 		1 0 1 1.0E-01 0 0
CUI: C3715155
Disease: AMYOTROPHIC LATERAL SCLEROSIS 19
AMYOTROPHIC LATERAL SCLEROSIS 19 		1 0 1 1.0E-01 0 0
CUI: C3806670
Disease: PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 1
PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 1 		1 0 1 1.0E-01 0 0
CUI: C3827273
Disease: Sudden Unexplained Death in Childhood
Sudden Unexplained Death in Childhood 		1 0 1 1.0E-01 0 0
CUI: C4023511
Disease: Obtundation status
Obtundation status 		12 0 2 1.0E-01 0 0
CUI: C4225360
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 30
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 30 		1 0 1 1.0E-01 0 0
CUI: C4727684
Disease: Metastatic Oral Cavity Squamous Cell Carcinoma
Metastatic Oral Cavity Squamous Cell Carcinoma 		1 0 1 1.0E-01 0 0
CUI: C4751570
Disease: Ferro-cerebro-cutaneous syndrome
Ferro-cerebro-cutaneous syndrome 		1 0 1 1.0E-01 0 0
CUI: C4755310
Disease: Cryptogenic late-onset epileptic spasms
Cryptogenic late-onset epileptic spasms 		1 0 1 1.0E-01 0 0