{"orpha":2486,"name":"Transverse limb deficiency-hemangioma syndrome","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 Familial cerebral cavernous malformation","url":"https://raremap.alftech.space/d/ORPHA-2486/","orphanet_url":"https://www.orpha.net/en/disease/detail/2486","names":{"fr":{"name":"Syndrome d'anomalies transverses des membres-hémangiome"},"de":{"name":"Transversale Extremitätenfehlbildungen-Hämangiom-Syndrom"},"es":{"name":"Síndrome de anomalía de las extremidades transversa-hemangioma"},"it":{"name":"Anomalie trasversali degli arti - emangioma"},"nl":{"name":"Dwarse ledemaatdeficiëntie - hemangioom-syndroom"},"pt":{"name":"Síndrome de defeitos transversais dos membros-hemangioma"},"pl":{"name":"Skrócenie poprzeczne kończyn - hemangioma"},"cs":{"name":"Syndrom zahrnující transverzální končetinový deficit a hemangiom"},"uk":{"name":"Синдром поперечної гемангіоми кінцівок"},"zh":{"name":"横向肢端骨缺损-血管瘤综合征"},"tr":{"name":"Transvers ekstremite eksikliği-hemanjiyom sendromu"}},"xrefs":[],"associations":[{"type":"Moved to","orpha":221061,"name":"Familial cerebral cavernous malformation"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}