{"orpha":235832,"name":"Congenital vascular bone syndrome","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-235832/","orphanet_url":"https://www.orpha.net/en/disease/detail/235832","names":{"fr":{"name":"Syndrome vasculaire osseux congénital"},"de":{"name":"Gefäßknochensyndrom, kongenitales"},"es":{"name":"Síndrome óseo vascular congénito"},"it":{"name":"Sindrome vascolare ossea congenita"},"nl":{"name":"Congenitaal vasculair botsyndroom"},"pt":{"name":"Síndrome de osso vascular congénito"},"pl":{"name":"Wrodzony zespół waskularyzacji kości"},"cs":{"name":"Vrozený vaskulární syndrom kostí"},"uk":{"name":"Вроджений судинно-кістковий синдром"},"zh":{"name":"先天性血管骨综合征"},"tr":{"name":"Doğumsal vasküler kemik sendromu"}},"xrefs":[{"source":"ICD-11","code":"LD26.6","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"825559961"},{"source":"MONDO","code":"16524","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680924","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":235835,"name":"OBSOLETE: Congenital vascular bone syndrome with limb overgrowth","status":"inactive"},{"type":"Referred to","orpha":235838,"name":"OBSOLETE: Congenital vascular bone syndrome with limb shortening","status":"inactive"}],"preferential_parent":{"orpha":93419,"name":"Rare bone disease"},"parents":[{"orpha":93419,"name":"Rare bone disease","classifications":[199]},{"orpha":183524,"name":"Rare genetic bone disease","classifications":[156]}],"children":[{"orpha":140436,"name":"Familial intraosseous vascular malformation","type":"Disease"},{"orpha":73,"name":"Gorham-Stout disease","type":"Malformation syndrome"},{"orpha":715923,"name":"Intraosseous venous malformation","type":"Morphological anomaly"},{"orpha":90307,"name":"Parkes Weber syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}