SE-ATLAS

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