{"orpha":98258,"name":"OBSOLETE: Infantile 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-98258/","orphanet_url":"https://www.orpha.net/en/disease/detail/98258","names":{"fr":{"name":"OBSOLETE : Syndrome épileptique du nourrisson"},"de":{"name":"OBSOLET: Epilepsie-Syndrom, infantiles"},"es":{"name":"OBSOLETO: Síndrome epiléptico infantil"},"it":{"name":"OBSOLETO: Sindrome epilettica infantile"},"nl":{"name":"OBSOLEET: Infantiele epilepsiesyndroom"},"pt":{"name":"OBSOLETO: Síndrome epilepsia do lactente"},"pl":{"name":"NIEAKTUALNE: Zespół padaczkowy okresu niemowlęcego"},"cs":{"name":"NEAKTUÁLNÍ: Kojenecké epileptické syndromy"},"uk":{"name":"Синдром інфантильної епілепсії"},"zh":{"name":"婴幼儿癫痫综合征"},"tr":{"name":"İnfantil 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}