{"orpha":98115,"name":"OBSOLETE: Non-pore-loop channelopathy due to Cl- channel skeletal muscle Clc1 anomaly","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 Thomsen and Becker disease","url":"https://raremap.alftech.space/d/ORPHA-98115/","orphanet_url":"https://www.orpha.net/en/disease/detail/98115","names":{"fr":{"name":"OBSOLETE : 'Canalopathie non ''pore loop'' due à un défaut du canal chlorure du muscle squelettique Clc1'"},"de":{"name":"OBSOLET: Ionenkanalkrankheit bei skeletomuskulärem ClC1-Chloridkanaldefekt"},"es":{"name":"OBSOLETO: Canalopatía 'non-pore-loop' por una anomalía del canal de Cl- del músculo esquelético Clc1"},"it":{"name":"OBSOLETO: Canalopatia da difetti del canale del cloro CLC-1 nei muscoli scheletrici"},"nl":{"name":"OBSOLEET: Non-pore-loop-kanalopathie als gevolg van Cl-kanaal skeletspier Clc1-anomalie"},"pt":{"name":"OBSOLETO: Canalopatia não-\"pore-loop\" por anomalia do canal de cloro do músculo esquelético Clc1"},"pl":{"name":"NIEAKTUALNE: Defekt kanalów nie posiadajacych petli z powodu anomalii kanalu chlorkowego Clc1 w miesniach szkieletowych"},"cs":{"name":"NEAKTUÁLNÍ: Non-pore-loop kanalopatie způsobená Clc1 anomálií Cl- kanálů příčně pruhovaných svalů"},"uk":{"name":"ЗАСТАРІЛО: Каналопатія без порової петлі, зумовлена аномалією Cl- каналу скелетних мязів Clc1"},"zh":{"name":"弃用：氯离子通道骨骼肌Clc1亚型异常所致非孔-环离子通道病"},"tr":{"name":"Eski adı: Cl- kanal iskelet kası Clc1 anomalisine bağlı gözenek dışı kanal kanalatiği"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":614,"name":"Thomsen and Becker disease"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}