SE-ATLAS

ARX-related epileptic encephalopathy Action myoclonus-renal failure syndrome Acute encephalopathy with inflammation-mediated status epilepticus Adolescent-onset epilepsy syndrome Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome Audiogenic seizures Autosomal dominant epilepsy with auditory features Autosomal dominant nocturnal frontal lobe epilepsy Benign childhood occipital epilepsy, Gastaut type Benign childhood occipital epilepsy, Panayiotopoulos type Benign familial infantile epilepsy Benign familial mesial temporal lobe epilepsy Benign familial neonatal epilepsy Benign familial neonatal-infantile seizures Benign focal seizures of adolescence Benign idiopathic neonatal seizures Benign occipital epilepsy Benign partial epilepsy of infancy with complex partial seizures Benign partial epilepsy with secondarily generalized seizures in infancy Benign partial infantile seizures CDKL5-deficiency disorder CNTNAP2-related developmental and epileptic encephalopathy Celiac disease-epilepsy-cerebral calcification syndrome Cerebral diseases of vascular origin with epilepsy Cerebral malformation with epilepsy Childhood absence epilepsy Chromosomal anomaly with epilepsy as a major feature Continuous spikes and waves during sleep DEND syndrome Dravet syndrome Early infantile epileptic encephalopathy Early myoclonic encephalopathy Early-onset epilepsy-intellectual disability-brain anomalies syndrome Early-onset progressive encephalopathy with migrant continuous myoclonus Epilepsy and/or ataxia with myoclonus as a major feature Epilepsy syndrome Epilepsy with myoclonic absences Epilepsy-microcephaly-skeletal dysplasia syndrome Epilepsy-telangiectasia syndrome Epileptic encephalopathy with global cerebral demyelination Familial focal epilepsy with variable foci Familial infantile myoclonic epilepsy Familial mesial temporal lobe epilepsy with febrile seizures Familial partial epilepsy Familial temporal lobe epilepsy Female restricted epilepsy with intellectual disability Generalized epilepsy with febrile seizures-plus Generalized epilepsy-paroxysmal dyskinesia syndrome Idiopathic hemiconvulsion-hemiplegia syndrome Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes Infantile convulsions and choreoathetosis Infantile epilepsy syndrome Infantile epileptic-dyskinetic encephalopathy Infantile spasms syndrome Infantile spasms-broad thumbs syndrome Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression Infectious disease with epilepsy Inflammatory and autoimmune disease with epilepsy Juvenile absence epilepsy Juvenile myoclonic epilepsy KCNQ2-related epileptic encephalopathy Malignant migrating focal seizures of infancy Mesial temporal lobe epilepsy with hippocampal sclerosis Metabolic diseases with epilepsy Metal transport or utilization disorder with epilepsy Monogenic disease with epilepsy Moynahan syndrome Myoclonic epilepsy in non-progressive encephalopathies Myoclonic epilepsy of infancy Myoclonic-astatic epilepsy Neonatal epilepsy syndrome Neurocutaneous syndrome with epilepsy Non-specific early-onset epileptic encephalopathy Oculocerebrocutaneous syndrome Other metabolic disease with epilepsy PEHO syndrome PEHO-like syndrome Paroxysmal dyskinesia Progressive myoclonic epilepsy with dystonia Rare epilepsy Rolandic epilepsy Severe neonatal-onset encephalopathy with microcephaly Startle epilepsy Thinking seizures W syndrome X-linked epilepsy-learning disabilities-behavior disorders syndrome