{"orpha":93470,"name":"OBSOLETE: Dysharmonic micromelia","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 Primary bone dysplasia with micromelia","url":"https://raremap.alftech.space/d/ORPHA-93470/","orphanet_url":"https://www.orpha.net/en/disease/detail/93470","names":{"fr":{"name":"OBSOLETE : Micromélie dysharmonieuse"},"de":{"name":"OBSOLET: Mesomelie, dysharmonische"},"es":{"name":"OBSOLETO: Micromelia disarmónica"},"it":{"name":"OBSOLETO: Mesomelia disarmonica"},"nl":{"name":"OBSOLEET: Disharmonische micromelie"},"pt":{"name":"OBSOLETO: Micromelia desarmónica"},"pl":{"name":"NIEAKTUALNE: Mikromelia nieharmoniczna"},"cs":{"name":"NEAKTUÁLNÍ: Dysharmonická mikromelie"},"uk":{"name":"ЗАСТАРІЛО: Дисгармонійна мікромелія"},"zh":{"name":"弃用：非均一型短肢"},"tr":{"name":"Eski adı: Disharmonik mikromeli"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":364536,"name":"Primary bone dysplasia with micromelia"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}