{"orpha":98753,"name":"OBSOLETE: Autoimmune neurological channelopathy due to an acetylcholine receptor subunits defect","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 Autoimmune neurological channelopathy","url":"https://raremap.alftech.space/d/ORPHA-98753/","orphanet_url":"https://www.orpha.net/en/disease/detail/98753","names":{"fr":{"name":"OBSOLETE : Canalopathie neurologique auto-immune associé à un défaut de sous-unité du recepteur à l'acétylcholine"},"de":{"name":"OBSOLET: Ionenkanalkrankheit, autoimmune neurologische, bei Defekt einer Untereinheit des Acetylcholin-Rezeptors"},"es":{"name":"OBSOLETO: Canalopatía neurológica autoinmune por un defecto de las subunidades del receptor de la acetilcolina"},"it":{"name":"OBSOLETO: Canalopatia neurologica autoimmune da difetto delle subunità del recettore acetilcolinico"},"nl":{"name":"OBSOLEET: Auto-immune neurologische kanalopathie door een acetylcholinereceptor-subeenhedendefect"},"pt":{"name":"OBSOLETO: Canalopatia neurológica autoimune por defeito nas subunidades do recetor da acetilcolina"},"pl":{"name":"NIEAKTUALNE: Autoimmunologiczna kanalopatia neurologiczna z powodu defektu podjednostki receptora dla acetylocholiny"},"cs":{"name":"NEAKTUÁLNÍ: Autoimunitní kanálopatie způsobené poruchou podjednotek receptoru pro acetylcholin"},"uk":{"name":"ЗАСТАРІЛО: Аутоімунна неврологічна каналопатія, спричинена дефектом субодиниць ацетилхолінових рецепторів"},"zh":{"name":"乙酰胆碱受体亚基缺陷所致自身免疫性神经离子通道病"},"tr":{"name":"Eski adı: Bir asetilkolin reseptör alt birim defektine bağlı otoimmün nörolojik kanalopati"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":98750,"name":"Autoimmune neurological channelopathy"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}