{"orpha":98257,"name":"OBSOLETE: Neonatal epilepsy syndrome","type":"Category","group":"Group of disorders","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.<br/><br/>Instead, consider using Neonatal-infantile onset epilepsy syndrome","url":"https://raremap.alftech.space/d/ORPHA-98257/","orphanet_url":"https://www.orpha.net/en/disease/detail/98257","names":{"fr":{"name":"OBSOLETE : Syndrome épileptique du nouveau-né"},"de":{"name":"OBSOLET: Epilepsie-Syndrom, neonatales"},"es":{"name":"OBSOLETO: Síndrome epiléptico neonatal"},"it":{"name":"OBSOLETO: Sindrome epilettica neonatale"},"nl":{"name":"OBSOLEET: Neonatale epilepsiesyndroom"},"pt":{"name":"OBSOLETO: Síndrome epilepsia neonatal"},"pl":{"name":"NIEAKTUALNE: Zespół padaczkowy okresu noworodkowego"},"cs":{"name":"NEAKTUÁLNÍ: Novorozenecké epileptické syndromy"},"uk":{"name":"Синдром неонатальної епілепсії"},"zh":{"name":"新生儿癫痫综合征"},"tr":{"name":"Yenidoğan epilepsi sendromu"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":693802,"name":"Neonatal/infantile-onset epilepsy syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}