{"orpha":93437,"name":"Acromesomelic dysplasia","type":"Clinical group","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"definition":null,"note":"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.","url":"https://raremap.alftech.space/d/ORPHA-93437/","orphanet_url":"https://www.orpha.net/en/disease/detail/93437","names":{"fr":{"name":"Dysplasie acromésomélique"},"de":{"name":"Dysplasie, akromesomele"},"es":{"name":"Displasia acromesomélica"},"it":{"name":"Displasia acromesomelica"},"nl":{"name":"Acromesomele dysplasie"},"pt":{"name":"Displasia acromesomélica"},"pl":{"name":"Dysplazja akromezomeliczna"},"cs":{"name":"Akromezomelické dysplázie"},"uk":{"name":"Акромезотеліальна дисплазія"},"zh":{"name":"肢端肢中发育不全"},"tr":{"name":"Akromezomelik displazi"}},"xrefs":[{"source":"ICD-11","code":"LD24.9","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"2002361676"},{"source":"MONDO","code":"0019696","qualifier":"E","icd_relation":null,"validated":true},{"source":"MeSH","code":"C535658","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5235036","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"6","qualifier":"E","icd_relation":null,"validated":true},{"source":"MedDRA","code":"10083866","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93419,"name":"Rare bone disease"},"parents":[{"orpha":364526,"name":"Primary bone dysplasia","classifications":[147,156,199]}],"children":[{"orpha":2098,"name":"Acromesomelic dysplasia, Grebe type","type":"Malformation syndrome"},{"orpha":968,"name":"Acromesomelic dysplasia, Hunter-Thompson type","type":"Malformation syndrome"},{"orpha":40,"name":"Acromesomelic dysplasia, Maroteaux type","type":"Malformation syndrome"},{"orpha":93382,"name":"Brachydactyly type A6","type":"Malformation syndrome"},{"orpha":2639,"name":"Fibular aplasia-complex brachydactyly syndrome","type":"Malformation syndrome"},{"orpha":2496,"name":"Mesomelia-synostoses syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}