Source: BEFREE ×
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: C1839333
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2 		57 26 54 0.89 26 0.81
CUI: C4505072
Disease: Epileptic Syndromes
Epileptic Syndromes 		46 2 17 0.20 1 3.0E-02
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy 		133 33 24 0.14 2 3.2E-02
CUI: C0751495
Disease: Seizures, Focal
Seizures, Focal 		33 0 11 0.14 0 0
CUI: C4316903
Disease: Absence Seizures
Absence Seizures 		25 0 10 0.14 0 0
CUI: C3502809
Disease: Generalized Epilepsy with Febrile Seizures Plus
Generalized Epilepsy with Febrile Seizures Plus 		9 12 8 0.14 3 7.3E-02
CUI: C0014550
Disease: Myoclonic Epilepsy
Myoclonic Epilepsy 		58 0 13 0.13 0 0
CUI: C0014553
Disease: Absence Epilepsy
Absence Epilepsy 		80 17 15 0.12 1 2.1E-02
CUI: C0391958
Disease: Familial Epilepsies
Familial Epilepsies 		16 0 8 0.12 0 0
CUI: C0494475
Disease: Tonic - clonic seizures
Tonic - clonic seizures 		45 11 11 0.12 1 2.4E-02
CUI: C0270850
Disease: Idiopathic generalized epilepsy
Idiopathic generalized epilepsy 		91 0 15 0.11 0 0
CUI: C0014548
Disease: Epilepsy, Generalized
Epilepsy, Generalized 		73 0 13 0.11 0 0
CUI: C4552072
Disease: X-linked infantile spasms
X-linked infantile spasms 		44 0 10 0.11 0 0
CUI: C0159020
Disease: Convulsions in the newborn
Convulsions in the newborn 		16 0 7 0.10 0 0
CUI: C0220669
Disease: Familial benign neonatal epilepsy
Familial benign neonatal epilepsy 		18 0 7 0.10 0 0
CUI: C0270853
Disease: Juvenile Myoclonic Epilepsy
Juvenile Myoclonic Epilepsy 		73 0 12 0.10 0 0
CUI: C4281785
Disease: Childhood Absence Epilepsy
Childhood Absence Epilepsy 		31 0 8 9.9E-02 0 0
CUI: C1852581
Disease: EPILEPSY, BENIGN NEONATAL, 2
EPILEPSY, BENIGN NEONATAL, 2 		9 0 6 9.8E-02 0 0
CUI: C3889476
Disease: Benign Familial Convulsion
Benign Familial Convulsion 		9 0 6 9.8E-02 0 0
CUI: C0238111
Disease: Lennox-Gastaut syndrome
Lennox-Gastaut syndrome 		21 0 7 9.7E-02 0 0
CUI: C1833661
Disease: PAROXYSMAL EXTREME PAIN DISORDER
PAROXYSMAL EXTREME PAIN DISORDER 		10 0 6 9.7E-02 0 0
CUI: C3887898
Disease: Infantile Spasm
Infantile Spasm 		79 0 12 9.6E-02 0 0
CUI: C0234533
Disease: Generalized seizures
Generalized seizures 		45 0 9 9.6E-02 0 0
CUI: C0037769
Disease: West Syndrome
West Syndrome 		113 0 14 8.9E-02 0 0
CUI: C1719788
Disease: Episodic ataxia type 1
Episodic ataxia type 1 		16 0 6 8.8E-02 0 0