SE-ATLAS

CLN7-Krankheit Limbische Enzephalitis mit assoziierten Antikörpern gegen Zellwandantigene Epilepsie, seltene Polymikrogyrie, unilaterale Zöliakie-Epilepsie-zerebrale Verkalkungen-Syndrom Epileptische Enzephalopathie mit globaler zerebraler Demyelinisierung CLN2-Krankheit Schreckepilepsie Zerebrale Fehlbildung mit Epilepsie Enzephalopathie, Thiamin-responsive Kortikale Dysplasie, fokale isolierte, Typ II X-chromosomal-dominante Intelligenzminderung-Epilepsie-Syndrom Frühinfantile epileptische Enzephalopathie-kortikale Blindheit-Intelligenzminderung-Gesichtsdysmorphie-Syndrom Myoklonusepilepsie des Kindesalters Okulo-zerebro-kutanes Syndrom Fokale Epilepsie - Intelligenzminderung - zerebro-zerebelläre Fehlbildung Makrogyrie, bilaterale zentrale Frühinfantile epileptische Enzephalopathie und Intelligenzminderung durch GRIN2A-Genmutation Proteus-Syndrom Idiopathische Hemikonvulsion-Hemiplegie-Syndrom Fokalepilepsie, benigne infantile, mit Midline-Spikes und Waves im Schlaf Limbische Enzephalitis, akute, nach Transplantation Rett-Syndrom DEND-Syndrom Krämpfe, beninge infantile, assoziiert mit milder Gastroenteritis Myoklonusepilepsie, progressive, Typ 5 Epilepsie mit myoklonischen Absencen Familiäres Epilepsiesyndrom, idiopathisches oder kryptogenes, mit bekanntem Gen/-ort Ringchromosom-20-Syndrom Polymikrogyrie, bilaterale Lennox-Gastaut-Syndrom Hyper-beta-Alaninämie X-chromosomale Intelligenzminderung-Epilepsie-Syndrom Intelligenzminderung, X-chromosomale, Typ Hedera Holoprosenzephalie CLN1-Krankheit Polymikrogyrie, fokale unilaterale Partialepilepsie, benigne infantile Mikrodeletionssyndrom 15q13.3 Zerebrale Fehlbildung durch neuronalen Migrationsdefekt, nichtsyndromal Absencen-Epilepsie, juvenile Heterotopie, noduläre subependymale X-chromosomale Epilepsie mit Lernstörungen und Verhaltensauffälligkeiten Fieber-assoziierte Enzephalopathie mit refraktären Anfällen Rolando-Epilepsie-Sprachdyspraxie-Syndrom Neurokutanes Syndrom mit Epilepsie Krampfanfälle, benigne infantile nicht-familiäre Infantile mesiale Temporallappenepilepsie mit schwerer kognitiver Regression Myoklonische Epilepsie bei nicht-progressiven Enzephalopathien Epilepsie mit myoklonisch-astatischen Krisen Hemimegalenzephalie Aicardi-Syndrom Intermediäres DEND-Syndrom Heterotopie, noduläre subkortikale Autosomal-dominante fokale Epilepsie mit akustischen Merkmalen Infantile Konvulsionen und Choreoathetose Warmwasser-Reflexepilepsie Epileptische Syndrome Pachygyrie, frontotemporale, autosomal-rezessive Neurofibromatose Typ 1 durch NF1-Genmutation oder intragenische Deletion Autismus-Epilepsie-Syndrom durch Verzweigtketten-Ketosäuredehydrogenase-Kinase-Mangel Intelligenzminderung, X-chromosomale, syndromale, Typ Claes-Jensen Epilepsie, benigne familiäre infantile Ceroid-Lipofuszinose, neuronale, spät-infantile Enzephalopathie, epileptische, ARX-assoziierte Früh beginnende progressive Enzephalopathie mit wanderndem kontinuierlichem Myoklonus Moynahan-Syndrom Krampfanfälle, miktionsinduzierte Isolated focal cortical dysplasia type I Congenital rubella syndrome Juvenile myoclonic epilepsy Benign childhood occipital epilepsy, Panayiotopoulos type Septopreoptic holoprosencephaly Mesial temporal lobe epilepsy with hippocampal sclerosis Eating reflex epilepsy Progressive myoclonic epilepsy type 1 Paraneoplastic limbic encephalitis Solitary median maxillary central incisor syndrome Lissencephaly Benign partial epilepsy of infancy with complex partial seizures Limbic encephalitis with DPP6 antibodies Pachygyria-intellectual disability-epilepsy syndrome Infantile neuronal ceroid lipofuscinosis Corpus callosum agenesis-abnormal genitalia syndrome Benign adult familial myoclonic epilepsy Cryptogenic late-onset epileptic spasms Rasmussen subacute encephalitis Familial mesial temporal lobe epilepsy with febrile seizures CLN4A disease Cerebral diseases of vascular origin with epilepsy Epilepsy with eyelid myoclonia Reading seizures Klüver-Bucy syndrome Lobar holoprosencephaly Reflex epilepsy Benign occipital epilepsy Adult neuronal ceroid lipofuscinosis Colorado tick fever Acquired porencephaly Herpes simplex virus encephalitis Progressive epilepsy-intellectual disability syndrome, Finnish type Incontinentia pigmenti Neonatal epilepsy syndrome Infantile epilepsy syndrome Tuberous sclerosis complex Familial focal epilepsy with variable foci Inflammatory and autoimmune disease with epilepsy Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to WWOX deficiency Midline interhemispheric variant of holoprosencephaly Fetal cytomegalovirus syndrome Malignant migrating focal seizures of infancy Progressive myoclonic epilepsy with dystonia Eastern equine encephalitis CLN11 disease CLN10 disease Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to TUD deficiency Hereditary neurocutaneous malformation Microlissencephaly-micromelia syndrome Juvenile neuronal ceroid lipofuscinosis Neurofibromatosis type 1 Primary microcephaly-epilepsy-permanent neonatal diabetes syndrome Benign familial neonatal epilepsy Diffuse cerebral and cerebellar atrophy-intractable seizures-progressive microcephaly syndrome Adolescent-onset epilepsy syndrome Infectious disease with epilepsy PEHO syndrome Congenital toxoplasmosis Partington syndrome Early-onset Lafora body disease Progressive myoclonic epilepsy type 3 CLN13 disease Childhood-onset epilepsy syndrome Lafora disease Congenital neuronal ceroid lipofuscinosis Acute disseminated encephalomyelitis Infantile spasms syndrome Familial porencephaly W syndrome Epilepsy-telangiectasia syndrome Encephalitis lethargica Subcortical band heterotopia CLN4B disease Limbic encephalitis with nCMAgs antibodies EAST syndrome Pneumococcal meningitis Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome Ito hypomelanosis X-linked lissencephaly with abnormal genitalia Progressive myoclonic epilepsy Orgasm-induced seizures Monogenic disease with epilepsy Rubella panencephalitis Continuous spikes and waves during sleep Kleefstra syndrome due to 9q34 microdeletion Benign partial epilepsy with secondarily generalized seizures in infancy Limbic encephalitis with caspr2 antibodies Benign childhood occipital epilepsy, Gastaut type Familial temporal lobe epilepsy Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome CLN6 disease Photosensitive epilepsy CLN5 disease Audiogenic seizures Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN deficiency Atypical Rett syndrome Acute encephalopathy with biphasic seizures and late reduced diffusion La Crosse encephalitis Infantile epileptic-dyskinetic encephalopathy St. Louis encephalitis Partial corpus callosum agenesis-cerebellar vermis hypoplasia with posterior fossa cysts syndrome New-onset refractory status epilepticus Generalized epilepsy with febrile seizures-plus Progressive myoclonic epilepsy type 6 Acute encephalopathy with inflammation-mediated status epilepticus Bilateral parasagittal parieto-occipital polymicrogyria Bilateral generalized polymicrogyria Semilobar holoprosencephaly Schizencephaly Generalized epilepsy-paroxysmal dyskinesia syndrome Dravet syndrome Familial partial epilepsy Action myoclonus-renal failure syndrome Benign familial mesial temporal lobe epilepsy Early infantile epileptic encephalopathy Rolandic epilepsy Severe neonatal-onset encephalopathy with microcephaly Autosomal dominant nocturnal frontal lobe epilepsy CLN8 disease Landau-Kleffner syndrome CLN9 disease Benign focal seizures of adolescence Morvan syndrome West-Nile encephalitis Thinking seizures Mycoplasma encephalitis Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation Benign idiopathic neonatal seizures MERRF Limbic encephalitis Occipital pachygyria and polymicrogyria Chromosomal anomaly with epilepsy as a major feature Non-paraneoplastic limbic encephalitis Nodular neuronal heterotopia X-linked spasticity-intellectual disability-epilepsy syndrome Familial encephalopathy with neuroserpin inclusion bodies Benign familial neonatal-infantile seizures Sturge-Weber syndrome Western equine encephalitis Microform holoprosencephaly Polymicrogyria Isolated focal cortical dysplasia Cerebral cortical dysplasia Hyperekplexia-epilepsy syndrome Perioral myoclonia with absences Neuroectodermal melanolysosomal disease NMDA receptor encephalitis Constitutional megaloblastic anemia with severe neurologic disease Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome Unilateral hemispheric polymicrogyria Alobar holoprosencephaly Classic paraneoplastic limbic encephalitis Bilateral frontal polymicrogyria Limbic encephalitis with LGI1 antibodies Bilateral perisylvian polymicrogyria Periventricular nodular heterotopia Metabolic diseases with epilepsy Non-herpetic acute limbic encephalitis Infantile spasms-broad thumbs syndrome Female restricted epilepsy with intellectual disability Meningococcal meningitis Bilateral frontoparietal polymicrogyria Subacute sclerosing leukoencephalitis Childhood absence epilepsy Japanese encephalitis Tick-borne encephalitis Channelopathy with epilepsy Familial infantile myoclonic epilepsy CNTNAP2-related developmental and epileptic encephalopathy Hypothalamic hamartomas with gelastic seizures Porencephaly Early myoclonic encephalopathy 17q11 microdeletion syndrome Ring chromosome 14 syndrome PEHO-like syndrome