{"orpha":98469,"name":"OBSOLETE: Congenital muscular dystrophy due to glycosyltransferase 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 Congenital muscular dystrophy","url":"https://raremap.alftech.space/d/ORPHA-98469/","orphanet_url":"https://www.orpha.net/en/disease/detail/98469","names":{"fr":{"name":"OBSOLETE : Dystrophie musculaire congénitale par anomalie de la glycosyltransférase"},"de":{"name":"OBSOLET: Muskeldystrophie, kongenitale, durch Glykosyltransferase-Anomalie"},"es":{"name":"OBSOLETO: Distrofia muscular congénita por una anomalía de la glicosiltransferasa"},"it":{"name":"OBSOLETO: Distrofia muscolare congenita da anomalia delle glicosiltransferasi"},"nl":{"name":"OBSOLEET: Congenitale spierdystrofie door glycosyltransferaseanomalie"},"pt":{"name":"OBSOLETO: Distrofia muscular congénita por anomalia da glicosiltransferase"},"pl":{"name":"NIEAKTUALNE: Wrodzona dystrofia miesniowa z powodu anomalii glikozylotransferazy"},"cs":{"name":"NEAKTUÁLNÍ: Vrozená svalová dystrofie způsobená anomálií glykosyltransferázy"},"uk":{"name":"ЗАСТАРІЛО: Вроджена мязова дистрофія внаслідок аномалії глікозилтрансферази"},"zh":{"name":"弃用：糖基转移酶异常所致先天性肌营养不良"},"tr":{"name":"Eski adı: Glikosiltransferaz anomalisine bağlı doğumsal kas distrofisi"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":97242,"name":"Congenital muscular dystrophy"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}