SE-ATLAS

15q13.3 microdeletion syndrome ARX-related epileptic encephalopathy Acquired porencephaly Action myoclonus-renal failure syndrome Acute disseminated encephalomyelitis Acute encephalopathy with biphasic seizures and late reduced diffusion Acute encephalopathy with inflammation-mediated status epilepticus Adolescent-onset epilepsy syndrome Adult neuronal ceroid lipofuscinosis Aicardi syndrome Alobar holoprosencephaly Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome Atypical Rett syndrome Audiogenic seizures Autism-epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency Autosomal dominant epilepsy with auditory features Autosomal dominant nocturnal frontal lobe epilepsy Autosomal recessive frontotemporal pachygyria Baraitser-Winter cerebrofrontofacial syndrome Benign adult familial myoclonic 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 infantile focal epilepsy with midline spikes and waves during sleep Benign infantile seizures associated with mild gastroenteritis Benign non-familial infantile 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 Bilateral frontal polymicrogyria Bilateral frontoparietal polymicrogyria Bilateral generalized polymicrogyria Bilateral parasagittal parieto-occipital polymicrogyria Bilateral perisylvian polymicrogyria Bilateral polymicrogyria CLN1 disease CLN10 disease CLN11 disease CLN13 disease CLN2 disease CLN4A disease CLN4B disease CLN5 disease CLN6 disease CLN7 disease CLN8 disease CLN9 disease CNTNAP2-related developmental and epileptic encephalopathy Celiac disease-epilepsy-cerebral calcification syndrome Central bilateral macrogyria Cerebral cortical dysplasia Cerebral diseases of vascular origin with epilepsy Cerebral malformation with epilepsy Channelopathy with epilepsy Childhood absence epilepsy Childhood-onset epilepsy syndrome Chromosomal anomaly with epilepsy as a major feature Classic lissencephaly Classic paraneoplastic limbic encephalitis Cobblestone lissencephaly Cobblestone lissencephaly without muscular or ocular involvement Colorado tick fever Congenital muscular alpha-dystroglycanopathy with brain and eye anomalies Congenital muscular dystrophy, Fukuyama type Congenital neuronal ceroid lipofuscinosis Congenital rubella syndrome Congenital toxoplasmosis Constitutional megaloblastic anemia with severe neurologic disease Continuous spikes and waves during sleep Corpus callosum agenesis-abnormal genitalia syndrome Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation Craniotelencephalic dysplasia Cryptogenic late-onset epileptic spasms Cystic fibrosis DEND syndrome Dravet syndrome EAST syndrome Early infantile epileptic encephalopathy Early myoclonic encephalopathy Early-onset Lafora body disease Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation Early-onset progressive encephalopathy with migrant continuous myoclonus Eastern equine encephalitis Eating reflex epilepsy Encephalitis lethargica Epilepsy syndrome Epilepsy with eyelid myoclonia Epilepsy with myoclonic absences Epileptic encephalopathy with global cerebral demyelination Familial encephalopathy with neuroserpin inclusion bodies Familial focal epilepsy with variable foci Familial infantile myoclonic epilepsy Familial mesial temporal lobe epilepsy with febrile seizures Familial partial epilepsy Familial porencephaly Familial temporal lobe epilepsy Febrile infection-related epilepsy syndrome Female restricted epilepsy with intellectual disability Fetal cytomegalovirus syndrome Focal epilepsy-intellectual disability-cerebro-cerebellar malformation Generalized epilepsy with febrile seizures-plus Generalized epilepsy-paroxysmal dyskinesia syndrome Hemimegalencephaly Hereditary neurocutaneous malformation Herpes simplex virus encephalitis Holoprosencephaly Hot water reflex epilepsy Hyper-beta-alaninemia Hyperekplexia-epilepsy syndrome Hypothalamic hamartomas with gelastic seizures Idiopathic hemiconvulsion-hemiplegia syndrome Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes Incontinentia pigmenti Infantile convulsions and choreoathetosis Infantile epilepsy syndrome Infantile epileptic-dyskinetic encephalopathy Infantile neuronal ceroid lipofuscinosis 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 Intermediate DEND syndrome Isolated focal cortical dysplasia Isolated focal cortical dysplasia type I Isolated focal cortical dysplasia type II Isolated lissencephaly type 1 without known genetic defects Ito hypomelanosis Japanese encephalitis Juvenile absence epilepsy Juvenile myoclonic epilepsy Juvenile neuronal ceroid lipofuscinosis KDM5C-related syndromic X-linked intellectual disability Kleefstra syndrome due to 9q34 microdeletion Klüver-Bucy syndrome La Crosse encephalitis Lafora disease Landau-Kleffner syndrome Late infantile neuronal ceroid lipofuscinosis Lennox-Gastaut syndrome Limbic encephalitis Limbic encephalitis associated with antibodies to cell membrane antigens Limbic encephalitis with DPP6 antibodies Limbic encephalitis with LGI1 antibodies Limbic encephalitis with caspr2 antibodies Limbic encephalitis with nCMAgs antibodies Lissencephaly Lissencephaly due to TUBA1A mutation Lissencephaly syndrome, Norman-Roberts type Lissencephaly type 1 due to doublecortin gene mutation Lissencephaly type 3 Lissencephaly type 3-familial fetal akinesia sequence syndrome Lissencephaly type 3-metacarpal bone dysplasia syndrome Lissencephaly with cerebellar hypoplasia Lissencephaly with cerebellar hypoplasia type A Lissencephaly with cerebellar hypoplasia type B Lissencephaly with cerebellar hypoplasia type C Lissencephaly with cerebellar hypoplasia type D Lissencephaly with cerebellar hypoplasia type E Lissencephaly with cerebellar hypoplasia type F Lobar holoprosencephaly MERRF Malignant migrating focal seizures of infancy Meningococcal meningitis Mesial temporal lobe epilepsy with hippocampal sclerosis Metabolic diseases with epilepsy Micro syndrome Microform holoprosencephaly Microlissencephaly Microlissencephaly-micromelia syndrome Micturation-induced seizures Midline interhemispheric variant of holoprosencephaly Miller-Dieker syndrome Monogenic disease with epilepsy Morvan syndrome Moynahan syndrome Muscle-eye-brain disease Muscle-eye-brain disease with bilateral multicystic leucodystrophy Mycoplasma encephalitis Myoclonic epilepsy in non-progressive encephalopathies Myoclonic epilepsy of infancy Myoclonic-astatic epilepsy NMDA receptor encephalitis Neonatal epilepsy syndrome Neu-Laxova syndrome Neurocutaneous syndrome with epilepsy Neuroectodermal melanolysosomal disease New-onset refractory status epilepticus Nodular neuronal heterotopia Non-herpetic acute limbic encephalitis Non-paraneoplastic limbic encephalitis Non-syndromic cerebral malformation due to abnormal neuronal migration OBSOLETE: CLN3 disease Occipital pachygyria and polymicrogyria Oculocerebrocutaneous syndrome Orgasm-induced seizures Other syndrome with lissencephaly as a major feature PEHO syndrome PEHO-like syndrome Pachygyria-intellectual disability-epilepsy syndrome Paraneoplastic limbic encephalitis Partington syndrome Perioral myoclonia with absences Periventricular nodular heterotopia Photosensitive epilepsy Pneumococcal meningitis Polymicrogyria Polymicrogyria due to TUBB2B mutation Polymicrogyria with optic nerve hypoplasia Porencephaly Posttransplant acute limbic encephalitis Primary microcephaly-epilepsy-permanent neonatal diabetes syndrome Progressive epilepsy-intellectual disability syndrome, Finnish type Progressive hemifacial atrophy Progressive myoclonic epilepsy Progressive myoclonic epilepsy type 1 Progressive myoclonic epilepsy type 3 Progressive myoclonic epilepsy type 6 Progressive myoclonic epilepsy with dystonia Proteus syndrome Rare epilepsy Rasmussen subacute encephalitis Reading seizures Reflex epilepsy Rett syndrome Ring chromosome 14 syndrome Ring chromosome 20 syndrome Rolandic epilepsy Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome Rolandic epilepsy-speech dyspraxia syndrome Rubella panencephalitis Schizencephaly Semilobar holoprosencephaly Septopreoptic holoprosencephaly Severe neonatal-onset encephalopathy with microcephaly Solitary median maxillary central incisor syndrome St. Louis encephalitis Startle epilepsy Sturge-Weber syndrome Sub-cortical nodular heterotopia Subacute sclerosing leukoencephalitis Subcortical band heterotopia Subependymal nodular heterotopia Thiamine-responsive encephalopathy Thinking seizures Tick-borne encephalitis Unilateral focal polymicrogyria Unilateral hemispheric polymicrogyria Unilateral polymicrogyria W syndrome Walker-Warburg syndrome West-Nile encephalitis Western equine encephalitis X-linked dominant intellectual disability-epilepsy syndrome X-linked epilepsy-learning disabilities-behavior disorders syndrome X-linked intellectual disability, Hedera type X-linked intellectual disability-epilepsy syndrome X-linked lissencephaly with abnormal genitalia X-linked spasticity-intellectual disability-epilepsy syndrome