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: C3495874
Disease: Nonepileptic Seizures
Nonepileptic Seizures 		102 0 1 9.8E-03 0 0
CUI: C4505436
Disease: Generalized Absence Seizures
Generalized Absence Seizures 		102 0 1 9.8E-03 0 0
CUI: C0270844
Disease: Tonic Seizures
Tonic Seizures 		108 0 1 9.3E-03 0 0
CUI: C0751494
Disease: Convulsive Seizures
Convulsive Seizures 		117 0 1 8.5E-03 0 0
CUI: C0234535
Disease: Clonic Seizures
Clonic Seizures 		122 0 1 8.2E-03 0 0
CUI: C0037773
Disease: Spastic Paraplegia, Hereditary
Spastic Paraplegia, Hereditary 		123 0 1 8.1E-03 0 0
CUI: C4317123
Disease: Myoclonic Seizures
Myoclonic Seizures 		123 0 1 8.1E-03 0 0
CUI: C0035304
Disease: Retinal Degeneration
Retinal Degeneration 		125 0 1 8.0E-03 0 0
CUI: C0279530
Disease: Malignant Bone Neoplasm
Malignant Bone Neoplasm 		125 0 1 8.0E-03 0 0
CUI: C4025846
Disease: Abnormality of vision
Abnormality of vision 		127 0 1 7.9E-03 0 0
CUI: C0149958
Disease: Complex partial seizures
Complex partial seizures 		140 0 1 7.1E-03 0 0
CUI: C0025363
Disease: Mental Retardation, Psychosocial
Mental Retardation, Psychosocial 		142 0 1 7.0E-03 0 0
CUI: C0231686
Disease: Gait, Unsteady
Gait, Unsteady 		143 0 1 7.0E-03 0 0
CUI: C0270846
Disease: Epileptic drop attack
Epileptic drop attack 		143 0 1 7.0E-03 0 0
CUI: C0917816
Disease: Mental deficiency
Mental deficiency 		148 0 1 6.8E-03 0 0
CUI: C0684276
Disease: Hypsarrhythmia
Hypsarrhythmia 		152 0 1 6.6E-03 0 0
CUI: C0020796
Disease: Profound Mental Retardation
Profound Mental Retardation 		160 0 1 6.3E-03 0 0
CUI: C1836038
Disease: Poor head control
Poor head control 		162 0 1 6.2E-03 0 0
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement 		169 0 1 5.9E-03 0 0
CUI: C4048158
Disease: Convulsions
Convulsions 		174 0 1 5.7E-03 0 0
CUI: C0085612
Disease: Ventricular arrhythmia
Ventricular arrhythmia 		176 0 1 5.7E-03 0 0
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy 		187 126 1 5.3E-03 1 7.4E-03
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
Henoch-Schoenlein Purpura 		198 59 1 5.1E-03 1 1.4E-02
CUI: C4316903
Disease: Absence Seizures
Absence Seizures 		205 0 1 4.9E-03 0 0
CUI: C0150055
Disease: Chronic pain
Chronic pain 		207 0 1 4.8E-03 0 0