{"orpha":1792,"name":"Humerospinal dysostosis","type":"Disease","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 CHST3-related skeletal dysplasia","url":"https://raremap.alftech.space/d/ORPHA-1792/","orphanet_url":"https://www.orpha.net/en/disease/detail/1792","names":{"fr":{"name":"Dysostose huméro-spinale"},"de":{"name":"Dysostose, humerospinale"},"es":{"name":"Disostosis humero espinal"},"it":{"name":"Disostosi omerospinale"},"nl":{"name":"Humerospinale dysostose"},"pt":{"name":"Disostose umero-espinhal","synonyms":["Síndrome Kozlowski-Celermajer"]},"pl":{"name":"Dyzostoza ramienno-kręgowa"},"cs":{"name":"Humerospinální dysostóza"},"uk":{"name":"Плечолопатковий дизостоз"},"zh":{"name":"脊椎骨骺发育不良伴先天性关节脱臼"},"tr":{"name":"Humerospinal disostoz"}},"xrefs":[],"associations":[{"type":"Moved to","orpha":263463,"name":"CHST3-related skeletal dysplasia"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}