{"orpha":98470,"name":"OBSOLETE: Congenital muscular dystrophy due to proteins of the endoplasmic reticulum 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-98470/","orphanet_url":"https://www.orpha.net/en/disease/detail/98470","names":{"fr":{"name":"OBSOLETE : Dystrophie musculaire congénitale par anomalie des protéines du réticulum endoplasmique"},"de":{"name":"OBSOLET: Muskeldystrophie, kongenitale, durch Proteinanomalie des endoplasmatischen Retikulums"},"es":{"name":"OBSOLETO: Distrofia muscular congénita por una anomalía de las proteínas del retículo endoplasmático"},"it":{"name":"OBSOLETO: Distrofia muscolare congenita da anomalia delle proteine del reticolo endoplasmatico"},"nl":{"name":"OBSOLEET: Congenitale spierdystrofie door anomalie van eiwitten van endoplasmische reticulum"},"pt":{"name":"OBSOLETO: Distrofia muscular congénita por anomalia de proteínas do retículo endoplasmático"},"pl":{"name":"NIEAKTUALNE: Wrodzona dystrofia miesniowa z powodu anomalii bialek retikulum endoplazmatycznego"},"cs":{"name":"NEAKTUÁLNÍ: Vrozená svalová dystrofie způsobená anomálií proteinů endoplazmatického retikula"},"uk":{"name":"ЗАСТАРІЛО: Вроджена мязова дистрофія, спричинена аномалією білків ендоплазматичного ретикулуму"},"zh":{"name":"弃用：内质网蛋白异常所致先天性肌营养不良"},"tr":{"name":"Eski adı: Endoplazmik retikulum anomalisinin proteinlerine 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}