Select item 4506 Epilepsy Seizure Disorders Seizure disorder Select item 766773 Epilepsy, idiopathic generalized, susceptibility to, 12 Select item 414549 Epilepsy, idiopathic generalized, susceptibility to, 8 Epilepsy, idiopathic generalized 8 Select item 416407 Epilepsy, idiopathic generalized, susceptibility to, 11 CLCN2-Related Juvenile Myoclonic Epilepsy Select item 155923 Unverricht-Lundborg syndrome EPILEPSY, PROGRESSIVE MYOCLONIC, 1A Epilepsy, progressive myoclonic 1A (Unverricht and Lundborg) Epilepsy, progressive myoclonic type 1 Epilepsy, progressive myoclonus 1 Myoclonic epilepsy of Unverricht and Lundborg Myoclonus progressive epilepsy of Unverricht and Lundborg Progressive myoclonus epilepsy baltic myoclonic epilepsy Unverricht-Lundborg Disease Select item 148243 Severe myoclonic epilepsy in infancy DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 6A Dravet syndrome Epilepsy, Myoclonic, Infantile, Severe Epileptic encephalopathy, early infantile, 6 (Dravet syndrome) Select item 155630 Dentatorubral-pallidoluysian atrophy Ataxia, chorea, seizures, and dementia Haw River syndrome Myoclonic epilepsy with choreoathetosis Naito Oyanagi disease Select item 440896 Epilepsy, childhood absence, susceptibility to, 6 Epilepsy, childhood absence 6 Select item 413424 Epilepsy, idiopathic generalized, susceptibility to, 9 CACNB4-Related Juvenile Myoclonic Epilepsy Epilepsy, idiopathic generalized 9 Select item 340341 Pyridoxine-dependent epilepsy EPILEPSY, EARLY-ONSET, 4, VITAMIN B6-DEPENDENT Pyridoxine dependency Pyridoxine dependency with seizures Pyridoxine-Dependent Seizures Vitamin B6-dependent seizures Select item 861910 Epilepsy, idiopathic generalized, susceptibility to, 13 EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 5 Epilepsy, juvenile myoclonic 5 Select item 460425 Seizures, benign familial neonatal, 1 Benign Neonatal Epilepsy 1 KCNQ2-Related Benign Familial Neonatal Epilepsy Select item 79465 Landau-Kleffner syndrome APHASIA, ACQUIRED, WITH EPILEPSY Acquired aphasia with convulsive disorder Acquired epileptiform aphasia EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT Epilepsy with neurodevelopmental defects Select item 330866 Childhood onset GLUT1 deficiency syndrome 2 Dystonia 18 GLUT1 deficiency syndrome 2 PAROXYSMAL EXERCISE-INDUCED DYSKINESIA WITH OR WITHOUT EPILEPSY AND/OR HEMOLYTIC ANEMIA PAROXYSMAL EXERTION-INDUCED DYSTONIA WITH OR WITHOUT EPILEPSY AND/OR HEMOLYTIC ANEMIA PED WITH OR WITHOUT EPILEPSY AND/OR HEMOLYTIC ANEMIA Paroxysmal exercise-induced dystonia Paroxysmal exertion-induced dyskinesia PxMD-SLC2A1 Select item 442800 Epilepsy, idiopathic generalized, susceptibility to, 7 EIG7 EJM2-Related Juvenile Myoclonic Epilepsy Epilepsy, idiopathic generalized 7 Select item 355328 Neuronal ceroid lipofuscinosis 8 northern epilepsy variant EPILEPSY, PROGRESSIVE, WITH MENTAL RETARDATION Northern epilepsy Select item 388117 Generalized epilepsy with febrile seizures plus, type 2 GEFS+, TYPE 2 SCN1A- Related Generalized Epilepsy with Febrile Seizures Plus Select item 1643229 Epilepsy, familial temporal lobe, 1 Autosomal Dominant Partial Epilepsy with Auditory Features Select item 155631 Lafora disease Epilepsy progressive myoclonic 2 Lafora body disorder Myoclonic epilepsy of Lafora Progressive Myoclonus Epilepsy, Lafora Type Select item 375302 Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis C10orf2-Related Ataxia Neuropathy Spectrum Disorders Epilepsy, progressive myoclonic, type 5 POLG-Related Ataxia Neuropathy Spectrum Disorders SENSORY ATAXIC NEUROPATHY WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome