{"orpha":1956,"name":"OBSOLETE: Erythromelalgia","type":"Disease","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 Primary erythromelalgia","url":"https://raremap.alftech.space/d/ORPHA-1956/","orphanet_url":"https://www.orpha.net/en/disease/detail/1956","names":{"fr":{"name":"OBSOLETE : Erythromélalgie"},"de":{"name":"OBSOLET: Erythromelalgie"},"es":{"name":"OBSOLETO: Eritromelalgia"},"it":{"name":"OBSOLETO: Eritromelalgia"},"nl":{"name":"OBSOLEET: Erytromelalgie"},"pt":{"name":"OBSOLETO: Eritromelalgia"},"pl":{"name":"NIEAKTUALNE: Erytromelalgia"},"cs":{"name":"NEAKTUÁLNÍ: Erytromelalgie"},"uk":{"name":"ЗАСТАРІЛО: Еритромелалгія"},"zh":{"name":"弃用：红斑性肢痛症"},"tr":{"name":"Eski adı: Eritromelalji"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":90026,"name":"Primary erythromelalgia"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}