{"orpha":715923,"name":"Intraosseous venous malformation","type":"Morphological anomaly","group":"Disorder","status":"active","flags":[],"synonyms":["Low-flow vascular malformation of the bone","IOVM"],"definition":null,"note":null,"url":"https://raremap.alftech.space/d/ORPHA-715923/","orphanet_url":"https://www.orpha.net/en/disease/detail/715923","names":{"fr":{"name":"Malformation veineuse osseuse","synonyms":["IOVM"]},"de":{"name":"Intraossäre venöse Fehlbildung","synonyms":["IOVM","Intraossäre venöse Malformation","Low-flow vaskuläre Malformation des Knochens"]},"es":{"name":"Malformación venosa intraósea","synonyms":["IOVM","Malformación vascular ósea de bajo flujo"]},"it":{"name":"Malformazione venosa intraossea","synonyms":["Malformazione vascolare dell'osso a basso flusso","IOVM","Malformazione vascolare ossea a basso flusso"]},"nl":{"name":"Intraossale veneuze malformatie","synonyms":["Low-flow vasculaire malformatie van bot","IOVM","Vaatmalformatie van bot met trage bloedstroom"]},"pt":{"name":"Intraosseous venous malformation"},"pl":{"name":"Śródkostna malformacja żylna","synonyms":["Low-flow vascular malformation of the bone","IOVM"]},"cs":{"name":"Intraosseous venous malformation","synonyms":["Low-flow vascular malformation of the bone","IOVM"]}},"xrefs":[{"source":"ICD-10","code":"Q27.8","qualifier":"NTBT","icd_relation":"attributed","validated":true},{"source":"ICD-11","code":"LA90.2Y","qualifier":"NTBT","icd_relation":"attributed","validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":235832,"name":"Congenital vascular bone syndrome","classifications":[156,199]},{"orpha":715334,"name":"Unifocal peripheral venous malformation","classifications":[147,198]}],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":["Autosomal recessive"],"onset":["Antenatal","Neonatal"],"prevalence":[{"type":"Point prevalence","qualification":"Class only","class":"Unknown","value":0.0,"area":"Worldwide","status":"Validated","source":"ORPHANET"}],"phenotypes":null}