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: C0544645
Disease: Focal Sensory Seizure
Focal Sensory Seizure 		2 0 2 0.33 0 0
CUI: C0403654
Disease: Bladder outflow obstruction
Bladder outflow obstruction 		5 0 2 0.22 0 0
CUI: C1719788
Disease: Episodic ataxia type 1
Episodic ataxia type 1 		16 0 4 0.22 0 0
CUI: C0220669
Disease: Familial benign neonatal epilepsy
Familial benign neonatal epilepsy 		19 0 4 0.19 0 0
CUI: C3502809
Disease: Generalized Epilepsy with Febrile Seizures Plus
Generalized Epilepsy with Febrile Seizures Plus 		13 0 3 0.19 0 0
CUI: C0238014
Disease: Acute cerebellar ataxia
Acute cerebellar ataxia 		1 0 1 0.17 0 0
CUI: C0393693
Disease: Benign Neonatal Epilepsy, Nonfamilial
Benign Neonatal Epilepsy, Nonfamilial 		1 0 1 0.17 0 0
CUI: C0863106
Disease: Afebrile seizure
Afebrile seizure 		8 0 2 0.17 0 0
CUI: C1834559
Disease: Continuous Muscle Fiber Activity, Hereditary
Continuous Muscle Fiber Activity, Hereditary 		1 0 1 0.17 0 0
CUI: C2363129
Disease: Benign Rolandic Epilepsy
Benign Rolandic Epilepsy 		15 0 3 0.17 0 0
CUI: C2674766
Disease: Myokymia 1
Myokymia 1 		1 0 1 0.17 0 0
CUI: C2677162
Disease: BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 9
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 9 		1 0 1 0.17 0 0
CUI: C2751195
Disease: Epilepsy, Benign Neonatal, 1, And-Or Myokymia
Epilepsy, Benign Neonatal, 1, And-Or Myokymia 		1 0 1 0.17 0 0
CUI: C3149074
Disease: SEIZURES, BENIGN FAMILIAL NEONATAL, 1
SEIZURES, BENIGN FAMILIAL NEONATAL, 1 		1 0 1 0.17 0 0
CUI: C3149075
Disease: SEIZURES, BENIGN FAMILIAL NEONATAL, 1, AND/OR MYOKYMIA
SEIZURES, BENIGN FAMILIAL NEONATAL, 1, AND/OR MYOKYMIA 		1 0 1 0.17 0 0
CUI: C3150986
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7 		1 0 1 0.17 0 0
CUI: C4016334
Disease: MYOKYMIA 1 WITH HYPOMAGNESEMIA
MYOKYMIA 1 WITH HYPOMAGNESEMIA 		1 0 1 0.17 0 0
CUI: C4511005
Disease: Autosomal dominant primary hypomagnesemia with hypocalciuria
Autosomal dominant primary hypomagnesemia with hypocalciuria 		1 0 1 0.17 0 0
CUI: C4539851
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 46
MENTAL RETARDATION, AUTOSOMAL DOMINANT 46 		1 0 1 0.17 0 0
CUI: C1852581
Disease: EPILEPSY, BENIGN NEONATAL, 2
EPILEPSY, BENIGN NEONATAL, 2 		9 20 2 0.15 1 4.8E-02
CUI: C3889476
Disease: Benign Familial Convulsion
Benign Familial Convulsion 		9 0 2 0.15 0 0
CUI: C0159020
Disease: Convulsions in the newborn
Convulsions in the newborn 		17 0 3 0.15 0 0
CUI: C0270862
Disease: Hemiplegic migraine
Hemiplegic migraine 		10 0 2 0.14 0 0
CUI: C2677843
Disease: Episodic Ataxia, Type 7
Episodic Ataxia, Type 7 		2 0 1 0.14 0 0
CUI: C3151685
Disease: Seizures in the newborn, refractory
Seizures in the newborn, refractory 		2 0 1 0.14 0 0