{"orpha":2641,"name":"OBSOLETE: Micromelic dwarfism, Fryns type","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 Spondylometaphyseal dysplasia","url":"https://raremap.alftech.space/d/ORPHA-2641/","orphanet_url":"https://www.orpha.net/en/disease/detail/2641","names":{"fr":{"name":"OBSOLETE : Nanisme micromélique type Fryns"},"de":{"name":"OBSOLET: Kleinwuchs, mikromeler, Typ Fryns"},"es":{"name":"OBSOLETO: Talla baja significativa micromélica tipo Fryns","synonyms":["OBSOLETO: Enanismo micromélico tipo Fryns"]},"it":{"name":"OBSOLETO: Nanismo micromelico, tipo Fryns"},"nl":{"name":"OBSOLEET: Micromelische dwerggroei, Fryns-type"},"pt":{"name":"OBSOLETO: Nanismo micromélico, tipo Fryns"},"pl":{"name":"NIEAKTUALNE: Niskoroslosc mikromeliczna typu Frynsa"},"cs":{"name":"NEAKTUÁLNÍ: Mikromelické trpaslictví, Frynsův typ"},"uk":{"name":"ЗАСТАРІЛО: Мікромелічна карликовість, тип Фрінса"},"zh":{"name":"弃用：细肢性侏儒症，Fryns型"},"tr":{"name":"Eski adı: Mikromelik cücelik, Fryns tipi"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":254,"name":"Spondylometaphyseal dysplasia"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}