{"orpha":98124,"name":"OBSOLETE: Channelopathy due to a skeletal muscle acetylcholine receptor 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 Congenital myasthenic syndrome","url":"https://raremap.alftech.space/d/ORPHA-98124/","orphanet_url":"https://www.orpha.net/en/disease/detail/98124","names":{"fr":{"name":"OBSOLETE : Canalopathie associée à un défaut du recepteur musculaire à l'acétylcholine"},"de":{"name":"OBSOLET: Ionenkanalkrankheit bei skeletomuskulärem ACh-Rezeptordefekt"},"es":{"name":"OBSOLETO: Canalopatía por un defecto del receptor de acetilcolina del músculo esquelético"},"it":{"name":"OBSOLETO: Canalopatia da difetti del recettore Ach nel muscolo scheletrico"},"nl":{"name":"OBSOLEET: Kanalopathie als gevolg van een skeletspier acetylcholinereceptordefect"},"pt":{"name":"OBSOLETO: Canalopatia por defeito do recetor da acetilcolina do músculo esquelético"},"pl":{"name":"NIEAKTUALNE: Kanalopatia z powodu defektu receptora acetylocholiny w miesniach szkieletowych"},"cs":{"name":"NEAKTUÁLNÍ: Kanalopatie způsobená poruchou acetylcholinových receptorů kosterních svalů"},"uk":{"name":"ЗАСТАРІЛО: Каналопатія внаслідок дефекту ацетилхолінових рецепторів скелетних мязів"},"zh":{"name":"弃用：骨骼肌乙酰胆碱受体缺陷离子通道病"},"tr":{"name":"Eski adı: İskelet kası asetilkolin reseptör defektine bağlı kanalopati"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":590,"name":"Congenital myasthenic syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}