SE-ATLAS

Lissencephaly Corpus callosum agenesis-abnormal genitalia syndrome Neonatal epilepsy syndrome Benign occipital epilepsy Rolandic epilepsy-speech dyspraxia syndrome Incontinentia pigmenti Childhood-onset epilepsy syndrome Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome Microform holoprosencephaly Infantile epilepsy syndrome Progressive myoclonic epilepsy Meningococcal meningitis Adolescent-onset epilepsy syndrome Dravet syndrome Proteus syndrome Acute encephalopathy with biphasic seizures and late reduced diffusion Lennox-Gastaut syndrome Benign childhood occipital epilepsy, Panayiotopoulos type Infantile convulsions and choreoathetosis Epilepsy syndrome Progressive myoclonic epilepsy type 6 Sturge-Weber syndrome Limbic encephalitis with caspr2 antibodies Benign childhood occipital epilepsy, Gastaut type Benign adult familial myoclonic epilepsy Chromosomal anomaly with epilepsy as a major feature Pachygyria-intellectual disability-epilepsy syndrome Familial temporal lobe epilepsy Landau-Kleffner syndrome Malignant migrating focal seizures of infancy New-onset refractory status epilepticus Microlissencephaly-micromelia syndrome Monogenic disease with epilepsy Familial focal epilepsy with variable foci EAST syndrome Porencephaly Ring chromosome 14 syndrome W syndrome Thiamine-responsive encephalopathy Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome Cerebral malformation with epilepsy Subacute sclerosing leukoencephalitis Occipital pachygyria and polymicrogyria Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes Acute encephalopathy with inflammation-mediated status epilepticus Isolated focal cortical dysplasia Ring chromosome 20 syndrome Hyper-beta-alaninemia Metabolic diseases with epilepsy Non-syndromic cerebral malformation due to abnormal neuronal migration Autosomal recessive frontotemporal pachygyria Lobar holoprosencephaly Paraneoplastic limbic encephalitis Limbic encephalitis with DPP6 antibodies Limbic encephalitis Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to TUD deficiency Midline interhemispheric variant of holoprosencephaly Inflammatory and autoimmune disease with epilepsy Classic paraneoplastic limbic encephalitis Alobar holoprosencephaly Primary microcephaly-epilepsy-permanent neonatal diabetes syndrome Infectious disease with epilepsy Constitutional megaloblastic anemia with severe neurologic disease Lafora disease Early-onset Lafora body disease Familial mesial temporal lobe epilepsy with febrile seizures Cerebral diseases of vascular origin with epilepsy Epileptic encephalopathy with global cerebral demyelination Atypical Rett syndrome Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN deficiency Limbic encephalitis associated with antibodies to cell membrane antigens Celiac disease-epilepsy-cerebral calcification syndrome Subcortical band heterotopia Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation Rett syndrome Hemimegalencephaly Sub-cortical nodular heterotopia Limbic encephalitis with LGI1 antibodies Subependymal nodular heterotopia Nodular neuronal heterotopia Solitary median maxillary central incisor syndrome PEHO-like syndrome Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome Hereditary neurocutaneous malformation Familial porencephaly Generalized epilepsy with febrile seizures-plus PEHO syndrome Limbic encephalitis with nCMAgs antibodies Female restricted epilepsy with intellectual disability Partington syndrome Polymicrogyria Semilobar holoprosencephaly Unilateral polymicrogyria Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation Central bilateral macrogyria X-linked intellectual disability, Hedera type Rare epilepsy X-linked dominant intellectual disability-epilepsy syndrome Non-paraneoplastic limbic encephalitis Non-herpetic acute limbic encephalitis CLN11 disease Holoprosencephaly Autosomal dominant epilepsy with auditory features NMDA receptor encephalitis Schizencephaly Bilateral polymicrogyria Posttransplant acute limbic encephalitis Moynahan syndrome Eastern equine encephalitis Progressive hemifacial atrophy Western equine encephalitis Tuberous sclerosis complex Unilateral focal polymicrogyria Acute disseminated encephalomyelitis Colorado tick fever Kleefstra syndrome due to 9q34 microdeletion Cerebral cortical dysplasia Isolated focal cortical dysplasia type I Encephalitis lethargica Morvan syndrome ARX-related epileptic encephalopathy Mesial temporal lobe epilepsy with hippocampal sclerosis Familial encephalopathy with neuroserpin inclusion bodies Channelopathy with epilepsy Bilateral frontoparietal polymicrogyria CLN13 disease Bilateral perisylvian polymicrogyria Progressive myoclonic epilepsy type 3 MERRF West-Nile encephalitis Progressive myoclonic epilepsy type 5 Unilateral hemispheric polymicrogyria Pneumococcal meningitis Periventricular nodular heterotopia Rubella panencephalitis CNTNAP2-related developmental and epileptic encephalopathy Partial corpus callosum agenesis-cerebellar vermis hypoplasia with posterior fossa cysts syndrome Mykoplasmen-Enzephalitis Okulo-zerebro-kutanes Syndrom Epilepsie, photosensitive CLN1-Krankheit St.-Louis-Enzephalitis Fokale Epilepsie - Intelligenzminderung - zerebro-zerebelläre Fehlbildung Schwere neonatale Enzephalopathie mit Mikrozephalie Kalifornische Enzephalitis Intermediäres DEND-Syndrom Infantile mesiale Temporallappenepilepsie mit schwerer kognitiver Regression Myoklonusepilepsie, infantile familiäre Warmwasser-Reflexepilepsie Rötelnembryopathie Ceroid-Lipofuszinose, neuronale, adulte CLN4A-Krankheit Ess-Reflexepilepsie Myoklonusepilepsie, progressive, mit Dystonie Ceroid-Lipofuszinose, neuronale, juvenile Reflexepilepsie, audiogene Rasmussen-Enzephalitis Herpes-simplex-Enzephalitis Klüver-Bucy-Syndrom CLN10-Krankheit Fetales Zytomegalie-Syndrom Ceroid-Lipofuszinose, neuronale, infantile Krampfanfälle, Orgasmus-induzierte CLN4B-Krankheit Hypothalamus-Hamartom mit gelastischen Anfällen Zeckenenzephalitis Enzephalopathie, epileptische, frühinfantile Form Idiopathische Hemikonvulsion-Hemiplegie-Syndrom DEND-Syndrom Enzephalopathie, frühkindliche myoklonische Hypomelanose Typ Ito Kortikale Dysplasie, fokale isolierte, Typ II Schreckepilepsie OBSOLET: CLN3-Krankheit Aktionsmyoklonus-Nierenversagen-Syndrom Myoklonusepilepsie des Kindesalters Neuroektodermale melanolysosomale Krankheit Denkepilepsie X-chromosomale Intelligenzminderung-Epilepsie-Syndrom Krampfanfälle, miktionsinduzierte Myoklonische Epilepsie bei nicht-progressiven Enzephalopathien Fieber-assoziierte Enzephalopathie mit refraktären Anfällen Generalisierte Epilepsie-paroxysmale Dyskinesie-Syndrom Epilepsie mit myoklonischen Absencen Absencen-Epilepsie, juvenile Epilepsie mit myoklonisch-astatischen Krisen Epilepsie, benigne familiäre infantile Neugeborenenkrämpfe, benigne idiopathische Autismus-Epilepsie-Syndrom durch Verzweigtketten-Ketosäuredehydrogenase-Kinase-Mangel Japanische Enzephalitis CLN2-Krankheit Früh beginnende progressive Enzephalopathie mit wanderndem kontinuierlichem Myoklonus Myoklonusepilepsie, juvenile CLN9-Krankheit Polymikrogyrie, bilaterale frontale Epilepsie, myoklonische progressive, Typ 1 Intelligenzminderung, X-chromosomale, syndromale, Typ Claes-Jensen Benigne Partialepilepsie im Kleinkindalter mit komplexen fokalen Anfällen Rolando-Epilepsie Infantile Krampfanfälle - breite Daumen Periorale Myoklonie mit Absencen Epilepsie, familiäre partielle Polymikrogyrie, bilaterale parasagittale parieto-okzipitale Krampfanfälle, benigne infantile nicht-familiäre Nächtliche Frontallappenepilepsie, autosomal-dominante Krampfanfälle, benigne familiäre neonatal-infantile Leseepilepsie Reflexepilepsie, genetisch-bedingte Epilepsie, progressive - Intelligenzminderung, Finnischer Typ CLN8-Krankheit X-chromosomale Spastik-Intelligenzminderung-Epilepsie-Syndrom Porenzephalie, erworbene Benigne Partialepilepsie der frühen Kindheit mit sekundär generalisierten Anfällen Absencen-Epilepsie des Kindesalters Benigne familiäre Neugeborenenepilepsie Toxoplasmose, kongenitale Polymikrogyrie, bilaterale generalisierte Zystische Fibrose CLN5-Krankheit Enzephalopathie, epileptisch-dyskinetische infantile Jeavons-Syndrom Epilepsie, kryptogenetische, spät beginnende Epilepsie-Teleangiektasie-Syndrom West-Syndrom Diffuse zerebrale und zerebelläre Atrophie-Intraktable Krämpfe-progressive Mikrozephalie-Syndrom Epilepsie mit kontinuierlichen Spike-Wave-Entladungen im Schlaf X-chromosomale Lissenzephalie mit Genitalanomalien Holoprosenzephalie, septopräoptische Benigne fokale Adoleszenten-Epilepsie CLN6-Krankheit Hyperekplexie - Epilepsie Ceroid-Lipofuszinose, neuronale, kongenitale Krämpfe, beninge infantile, assoziiert mit milder Gastroenteritis Autosomal-rezessive zerebelläre Ataxie - Epilepsie - Intelligenzminderung Mikrodeletionssyndrom 15q13.3 Partialepilepsie, benigne infantile Temporallappenepilepsie, mesiale, familiäre Form Ceroid-Lipofuszinose, neuronale, spät-infantile Aicardi-Syndrom Fokalepilepsie, benigne infantile, mit Midline-Spikes und Waves im Schlaf X-chromosomale Epilepsie mit Lernstörungen und Verhaltensauffälligkeiten CLN7-Krankheit