{"orpha":98122,"name":"OBSOLETE: Channelopathy due to a neuronal glycine 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 Hereditary hyperekplexia","url":"https://raremap.alftech.space/d/ORPHA-98122/","orphanet_url":"https://www.orpha.net/en/disease/detail/98122","names":{"fr":{"name":"OBSOLETE : Canalopathie associée à un défaut du recepteur neuronal de la glycine"},"de":{"name":"OBSOLET: Ionenkanalkrankheit bei neuronalem Glycin-Rezeptordefekt"},"es":{"name":"OBSOLETO: Canalopatía por un defecto del receptor de glicina neuronal"},"it":{"name":"OBSOLETO: Canalopatia da difetti del recettore neuronale della glicina"},"nl":{"name":"OBSOLEET: Kanalopathie als gevolg van een neuronaal glycinereceptordefect"},"pt":{"name":"OBSOLETO: Canalopatia por defeito do recetor neuronal da glicina"},"pl":{"name":"NIEAKTUALNE: Kanalopatia z powodu defektu neuronalnego receptora glicynowego"},"cs":{"name":"NEAKTUÁLNÍ: Kanalopatie způsobená poruchou neuronálních glycinových receptorů"},"uk":{"name":"ЗАСТАРІЛО: Каналопатія внаслідок дефекту гліцинових рецепторів нейронів"},"zh":{"name":"弃用：神经元甘氨酸受体缺陷离子通道病"},"tr":{"name":"Eski adı: Nöronal glisin reseptör defektine bağlı kanal gelişimi"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":3197,"name":"Hereditary hyperekplexia"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}