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: C0020578
Disease: Hyperventilation
Hyperventilation
31 0 6 0.10 0 0
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
57 0 8 9.8E-02 0 0
CUI: C4023511
Disease: Obtundation status
Obtundation status
12 0 4 9.8E-02 0 0
Generalized Epilepsy with Febrile Seizures Plus
13 0 4 9.5E-02 0 0
CUI: C0751122
Disease: Infantile Severe Myoclonic Epilepsy
Infantile Severe Myoclonic Epilepsy
63 0 8 9.1E-02 0 0
CUI: C4551857
Disease: Juvenile Myoclonic Epilepsy of Janz
Juvenile Myoclonic Epilepsy of Janz
4 0 3 8.8E-02 0 0
CUI: C4552768
Disease: Myoclonic Epilepsy, Adolescent
Myoclonic Epilepsy, Adolescent
4 0 3 8.8E-02 0 0
CUI: C4553087
Disease: Myoclonic Epilepsy, Juvenile, 1
Myoclonic Epilepsy, Juvenile, 1
4 0 3 8.8E-02 0 0
CUI: C4553298
Disease: Impulsive Petit Mal Epilepsy
Impulsive Petit Mal Epilepsy
4 0 3 8.8E-02 0 0
EEG with spike-wave complexes (>3.5 Hz)
5 0 3 8.6E-02 0 0
CUI: C0497202
Disease: Abnormal ocular motility
Abnormal ocular motility
45 0 6 8.3E-02 0 0
CUI: C4085238
Disease: MYOCLONIC-ATONIC EPILEPSY
MYOCLONIC-ATONIC EPILEPSY
6 0 3 8.3E-02 0 0
CUI: C0520966
Disease: Abnormal coordination
Abnormal coordination
59 0 7 8.2E-02 0 0
CUI: C0240991
Disease: Ataxia, Sensory
Ataxia, Sensory
35 0 5 7.9E-02 0 0
CUI: C4316903
Disease: Absence Seizures
Absence Seizures
205 8 17 7.7E-02 1 5.0E-02
CUI: C0009952
Disease: Febrile Convulsions
Febrile Convulsions
192 65 16 7.7E-02 1 1.3E-02
CUI: C0238111
Disease: Lennox-Gastaut syndrome
Lennox-Gastaut syndrome
25 0 4 7.4E-02 0 0
CUI: C1844690
Disease: Limited knee extension
Limited knee extension
11 0 3 7.3E-02 0 0
CUI: C0426900
Disease: Tibial torsion
Tibial torsion
12 0 3 7.1E-02 0 0
CUI: C0752323
Disease: Focal Clonic Seizures
Focal Clonic Seizures
12 0 3 7.1E-02 0 0
Generalized cerebral atrophy/hypoplasia
14 0 3 6.8E-02 0 0
CUI: C0391957
Disease: idiopathic epilepsy
idiopathic epilepsy
30 0 4 6.8E-02 0 0
CUI: C0391958
Disease: Familial Epilepsies
Familial Epilepsies
16 0 3 6.5E-02 0 0
CUI: C0393702
Disease: Myoclonic Astatic Epilepsy
Myoclonic Astatic Epilepsy
16 0 3 6.5E-02 0 0
CUI: C1719788
Disease: Episodic ataxia type 1
Episodic ataxia type 1
16 0 3 6.5E-02 0 0