{"orpha":98125,"name":"OBSOLETE: Channelopathy due to a neuronal 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 Autosomal dominant nocturnal frontal lobe epilepsy","url":"https://raremap.alftech.space/d/ORPHA-98125/","orphanet_url":"https://www.orpha.net/en/disease/detail/98125","names":{"fr":{"name":"OBSOLETE : Canalopathie associée à un défaut du recepteur neuronal à l'acétylcholine"},"de":{"name":"OBSOLET: Ionenkanalkrankheit bei neuronalem ACh-Rezeptordefekt"},"es":{"name":"OBSOLETO: Canalopatía por un defecto del receptor de acetilcolina neuronal"},"it":{"name":"OBSOLETO: Canalopatia da difetti del recettore neuronale Ach"},"nl":{"name":"OBSOLEET: Kanalopathie als gevolg van een neuronaal acetylcholinereceptordefect"},"pt":{"name":"OBSOLETO: Canalopatia por defeito do recetor da acetilcolina neuronal"},"pl":{"name":"NIEAKTUALNE: Kanalopatia z powodu defektu neuronalnego receptora acetylocholiny"},"cs":{"name":"NEAKTUÁLNÍ: Kanalopatie způsobená poruchou neuronálních acetylcholinových receptorů"},"uk":{"name":"ЗАСТАРІЛО: Каналопатія внаслідок дефекту ацетилхолінових рецепторів нейронів"},"zh":{"name":"弃用：神经元乙酰胆碱受体缺陷离子通道病"},"tr":{"name":"Eski adı: Nöronal asetilkolin reseptör defektine bağlı kanal gelişimi"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":98784,"name":"Sleep-related hypermotor epilepsy"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}