{"orpha":93301,"name":"Brachyolmia type 1, Hobaek type","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":[],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Autosomal recessive brachyolmia","url":"https://raremap.alftech.space/d/ORPHA-93301/","orphanet_url":"https://www.orpha.net/en/disease/detail/93301","names":{"fr":{"name":"Brachyolmie type 1 de Hobaek"},"de":{"name":"Brachyolmie Typ 1, Hobaek-Typ"},"es":{"name":"Braquiolmia tipo 1, tipo Hobaek"},"it":{"name":"Brachiolmia di Hobaek, tipo 1"},"nl":{"name":"Brachyolmie type 1, Hobaek-type"},"pt":{"name":"Braquiolmia tipo Hobaek"},"pl":{"name":"Brachyolmia typu 1, typu Hobaeka"},"cs":{"name":"Brachyolmie typ 1, Hobaekův typ"},"uk":{"name":"Брахіолмія типу 1, тип Хобаека"},"zh":{"name":"短躯干症，1型 Hobaek 型"},"tr":{"name":"Brakiyolmi tip 1, Hobaek tipi"}},"xrefs":[{"source":"OMIM","code":"271530","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":448242,"name":"Autosomal recessive brachyolmia"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}