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: C0751122
Disease: Infantile Severe Myoclonic Epilepsy
Infantile Severe Myoclonic Epilepsy
63 0 1 1.6E-02 0 0
CUI: C1849340
Disease: Long palpebral fissure
Long palpebral fissure
73 0 1 1.4E-02 0 0
CUI: C0236018
Disease: Aura
Aura
83 0 1 1.2E-02 0 0
CUI: C0751111
Disease: Awakening Epilepsy
Awakening Epilepsy
83 0 1 1.2E-02 0 0
CUI: C0086237
Disease: Epilepsy, Cryptogenic
Epilepsy, Cryptogenic
88 0 1 1.1E-02 0 0
Klinefelter's syndrome - male with more than two X chromosomes
90 0 1 1.1E-02 0 0
CUI: C0349506
Disease: Photosensitivity of skin
Photosensitivity of skin
91 0 1 1.1E-02 0 0
CUI: C0600104
Disease: Obsessive compulsive behavior
Obsessive compulsive behavior
94 0 1 1.1E-02 0 0
CUI: C0424230
Disease: Motor retardation
Motor retardation
98 0 1 1.0E-02 0 0
CUI: C4021759
Disease: Generalized myoclonic seizures
Generalized myoclonic seizures
105 0 1 9.5E-03 0 0
CUI: C3161330
Disease: Profound intellectual disabilities
Profound intellectual disabilities
112 0 1 8.9E-03 0 0
CUI: C0751494
Disease: Convulsive Seizures
Convulsive Seizures
117 0 1 8.5E-03 0 0
CUI: C0149958
Disease: Complex partial seizures
Complex partial seizures
140 0 1 7.1E-03 0 0
CUI: C1136249
Disease: Mental Retardation, X-Linked
Mental Retardation, X-Linked
141 0 1 7.1E-03 0 0
CUI: C0270846
Disease: Epileptic drop attack
Epileptic drop attack
143 0 1 7.0E-03 0 0
CUI: C0022735
Disease: Klinefelter Syndrome
Klinefelter Syndrome
150 0 1 6.7E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior
176 0 1 5.7E-03 0 0
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
187 0 1 5.3E-03 0 0
CUI: C0009952
Disease: Febrile Convulsions
Febrile Convulsions
192 0 1 5.2E-03 0 0
CUI: C4316903
Disease: Absence Seizures
Absence Seizures
205 0 1 4.9E-03 0 0
CUI: C0234533
Disease: Generalized seizures
Generalized seizures
210 0 1 4.8E-03 0 0
CUI: C0751495
Disease: Seizures, Focal
Seizures, Focal
210 0 1 4.8E-03 0 0
CUI: C0151611
Disease: Electroencephalogram abnormal
Electroencephalogram abnormal
227 0 1 4.4E-03 0 0
CUI: C0035372
Disease: Rett Syndrome
Rett Syndrome
234 0 1 4.3E-03 0 0
CUI: C0026351
Disease: Moderate intellectual disability
Moderate intellectual disability
251 0 1 4.0E-03 0 0