SE-ATLAS

Myoclonic epilepsy of infancy Idiopathic hemiconvulsion-hemiplegia syndrome 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 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 Lissencephaly with cerebellar hypoplasia type A Rolandic epilepsy Infantile spasms-broad thumbs syndrome 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 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 Cystic fibrosis Lissencephaly with cerebellar hypoplasia type D Childhood absence epilepsy Hyperekplexia-epilepsy syndrome Epilepsy with eyelid myoclonia 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 Benign familial mesial temporal lobe epilepsy Benign partial infantile seizures X-linked epilepsy-learning disabilities-behavior disorders syndrome Rolandic epilepsy-speech dyspraxia syndrome 15q13.3 microdeletion syndrome Aicardi syndrome Septopreoptic holoprosencephaly Lissencephaly Corpus callosum agenesis-abnormal genitalia syndrome Incontinentia pigmenti Micro syndrome Microform holoprosencephaly Childhood-onset epilepsy syndrome Meningococcal meningitis Progressive myoclonic epilepsy 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 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 Cerebral diseases of vascular origin with epilepsy Lobar holoprosencephaly Familial mesial temporal lobe epilepsy with febrile seizures Inflammatory and autoimmune disease with epilepsy 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 Atypical Rett syndrome Epileptic encephalopathy with global cerebral demyelination Celiac disease-epilepsy-cerebral calcification syndrome Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation Rett syndrome Lissencephaly syndrome, Norman-Roberts type Subependymal nodular heterotopia Hemimegalencephaly Sub-cortical nodular heterotopia 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 Cobblestone lissencephaly without muscular or ocular involvement Generalized epilepsy with febrile seizures-plus Hereditary neurocutaneous malformation Polymicrogyria due to TUBB2B mutation PEHO syndrome Familial porencephaly Polymicrogyria 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 X-linked intellectual disability, Hedera type Unilateral focal polymicrogyria Holoprosencephaly Schizencephaly Autosomal dominant epilepsy with auditory features NMDA receptor encephalitis Bilateral polymicrogyria Congenital muscular alpha-dystroglycanopathy with brain and eye anomalies Moynahan-Syndrom Westliche Pferdeenzephalitis Miller-Dieker-Syndrom Colorado-Zeckenfieber Hemiatrophia facialis progressiva Östliche Pferdeenzephalitis Enzephalomyelitis, akute disseminierte Sonstige Syndrome mit Lissenzephalie als Hauptmerkmal Lissenzephalie, klassische Kleefstra-Syndrom durch Mikrodeletion 9q34 Dysplasie, kortikale zerebrale Mikrolissenzephalie Lissenzephalie Typ 3 Lissenzephalie Typ 1, isolierte, ohne bekannten genetischen Defekt Kortikale Dysplasie, fokale isolierte, Typ I Encephalitis lethargica Baraitser-Winter zerebro-fronto-faziales Syndrom Morvan-Syndrom Muskeldystrophie, kongenitale, Typ Fukuyama Enzephalopathie, epileptische, ARX-assoziierte Mesiale Temporallappenepilepsie mit Hippocampussklerose Enzephalopathie mit Neuroserpin-Einschlüssen, familiäre Form Ionenkanalkrankheit mit Epilepsie Polymikrogyrie, bilaterale frontoparietale West-Nil-Enzephalitis MERRF Myoklonische Epilepsie, progressive, Typ 3 Polymikrogyrie, hemisphärische unilaterale Polymikrogyrie, bilaterale perisylvische Röteln-Panenzephalitis Heterotopie, noduläre periventrikuläre Pneumokokken-Meningitis Mykoplasmen-Enzephalitis CNTNAP2-assoziierte entwicklungsbedingte und epileptische Enzephalopathie Okzipitallappenepilepsie, photosensitive Polymikrogyrie mit Sehnerv-Hypoplasie Okulo-zerebro-kutanes Syndrom St.-Louis-Enzephalitis MECP2-assoziierte schwere neonatale Enzephalopathie Fokale Epilepsie-Intelligenzminderung-zerebro-zerebelläre Fehlbildung Kalifornische Enzephalitis Myoklonusepilepsie, infantile familiäre Intermediäres DEND-Syndrom TNK2-assoziierte Epilepsie mit schwerer kognitiver Rückentwicklung Reflexepilepsie, audiogene Muskel-Auge-Gehirn-Krankheit mit bilateraler multizystischer Leukodystrophie Rötelnembryopathie Warmwasser-Reflexepilepsie Ess-Reflexepilepsie Rasmussen-Enzephalitis Herpes-simplex-Enzephalitis Klüver-Bucy-Syndrom Fetales Zytomegalie-Syndrom Myoklonusepilepsie, progressive, mit Dystonie Cobblestone-Lissenzephalie Zeckenenzephalitis Frühinfantile entwicklungsbedingte und epileptische Enzephalopathie Epilepsie, Orgasmus-induzierte Enzephalopathie, frühkindliche myoklonische Hypothalamus-Hamartom mit gelastischen Anfällen