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: C1864987
Disease: Migraine, Familial Hemiplegic, 3
Migraine, Familial Hemiplegic, 3 		2 0 2 1.00 0 0
CUI: C4023408
Disease: Abnormality of mouth size
Abnormality of mouth size 		3 0 2 0.67 0 0
CUI: C1858673
Disease: GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2 		4 58 2 0.50 1 1.7E-02
CUI: C3264000
Disease: Refractory juvenile myoclonic epilepsy
Refractory juvenile myoclonic epilepsy 		1 0 1 0.50 0 0
CUI: C3827273
Disease: Sudden Unexplained Death in Childhood
Sudden Unexplained Death in Childhood 		1 0 1 0.50 0 0
CUI: C4551549
Disease: Early Infantile Epileptic Encephalopathy 6
Early Infantile Epileptic Encephalopathy 6 		4 0 2 0.50 0 0
CUI: C0393676
Disease: Panayiotopoulos Syndrome
Panayiotopoulos Syndrome 		2 0 1 0.33 0 0
CUI: C2751778
Disease: Generalized Epilepsy With Febrile Seizures Plus, 7
Generalized Epilepsy With Febrile Seizures Plus, 7 		2 0 1 0.33 0 0
CUI: C3151229
Disease: FEBRILE SEIZURES, FAMILIAL, 3B
FEBRILE SEIZURES, FAMILIAL, 3B 		2 0 1 0.33 0 0
CUI: C3281191
Disease: SCN8A-related epilepsy with encephalopathy
SCN8A-related epilepsy with encephalopathy 		2 0 1 0.33 0 0
CUI: C3698357
Disease: Refractory myoclonic epilepsy
Refractory myoclonic epilepsy 		2 0 1 0.33 0 0
CUI: C3805727
Disease: MEGALENCEPHALY, AUTOSOMAL DOMINANT
MEGALENCEPHALY, AUTOSOMAL DOMINANT 		6 0 2 0.33 0 0
CUI: C4012054
Disease: NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IID
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IID 		2 0 1 0.33 0 0
CUI: C0270857
Disease: Epilepsy, Reflex
Epilepsy, Reflex 		3 0 1 0.25 0 0
CUI: C0549118
Disease: Hemiplegia-hemiconvulsion-epilepsy syndrome
Hemiplegia-hemiconvulsion-epilepsy syndrome 		3 0 1 0.25 0 0
CUI: C0677600
Disease: Inspiratory stridor
Inspiratory stridor 		8 0 2 0.25 0 0
CUI: C1876181
Disease: EXTERNAL AUDITORY CANAL, BILATERAL ATRESIA OF, WITH CONGENITAL VERTICAL TALUS
EXTERNAL AUDITORY CANAL, BILATERAL ATRESIA OF, WITH CONGENITAL VERTICAL TALUS 		3 0 1 0.25 0 0
CUI: C0017332
Disease: Generalized Nonconvulsive Seizure Disorder
Generalized Nonconvulsive Seizure Disorder 		4 0 1 0.20 0 0
CUI: C0086236
Disease: Epilepsy, Atonic
Epilepsy, Atonic 		4 0 1 0.20 0 0
CUI: C0086241
Disease: Epilepsy, Tonic
Epilepsy, Tonic 		4 0 1 0.20 0 0
CUI: C0347869
Disease: Epilepsy, Akinetic
Epilepsy, Akinetic 		4 0 1 0.20 0 0
CUI: C1867971
Disease: Acute episodes of neuropathic symptoms
Acute episodes of neuropathic symptoms 		4 0 1 0.20 0 0
CUI: C4014430
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 21
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 21 		11 0 2 0.18 0 0
CUI: C0270854
Disease: Symptomatic Generalized Epilepsy
Symptomatic Generalized Epilepsy 		5 0 1 0.17 0 0
CUI: C0701811
Disease: Poor short-term memory
Poor short-term memory 		5 0 1 0.17 0 0