{"orpha":1819,"name":"OBSOLETE: Epimetaphyseal skeletal dysplasia","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Multiple metaphyseal dysplasia","url":"https://raremap.alftech.space/d/ORPHA-1819/","orphanet_url":"https://www.orpha.net/en/disease/detail/1819","names":{"fr":{"name":"OBSOLETE : Dysplasie épimétaphysaire autosomique dominante"},"de":{"name":"OBSOLET: Skelettdysplasie, epimetaphysäre dominante"},"es":{"name":"OBSOLETO: Displasia epimetafisaria dominante"},"it":{"name":"OBSOLETO: Displasia epimetafisaria dominante"},"nl":{"name":"OBSOLEET: Epimetafysaire skeletdysplasie"},"pt":{"name":"OBSOLETO: Displasia esquelética epimetafisária"},"pl":{"name":"NIEAKTUALNE: Szkieletowa dysplazja przynasadowa"},"cs":{"name":"NEAKTUÁLNÍ: Epimetafyzární skeletální dysplázie"},"uk":{"name":"ЗАСТАРІЛО: Епіметафізарна скелетна дисплазія"},"zh":{"name":"弃用：上干骺端骨发育不良"},"tr":{"name":"Eski adı: Epimetafizyal iskelet displazisi"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":93430,"name":"Multiple metaphyseal dysplasia"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}