{"orpha":714806,"name":"Multifocal sporadic venous malformation","type":"Morphological anomaly","group":"Disorder","status":"active","flags":[],"synonyms":["Multifocal VM"],"definition":null,"note":null,"url":"https://raremap.alftech.space/d/ORPHA-714806/","orphanet_url":"https://www.orpha.net/en/disease/detail/714806","names":{"fr":{"name":"Malformation veineuse multifocale sporadique","synonyms":["MV multifocale"]},"de":{"name":"Multifokale sporadische venöse Fehlbildung","synonyms":["Multifokale VM","Multifokale venöse Malformation"]},"es":{"name":"Malformación venosa esporádica multifocal","synonyms":["MAV multifocal"]},"it":{"name":"Malformazione venosa sporadica multifocale","synonyms":["MV multifocale"]},"nl":{"name":"Multifocale sporadische veneuze malformatie","synonyms":["Multifocale VM"]},"pt":{"name":"Multifocal sporadic venous malformation"},"pl":{"name":"Wieloogniskowa sporadyczna malformacja żylna","synonyms":["Multifocal VM"]},"cs":{"name":"Multifocal sporadic venous malformation","synonyms":["Multifocal VM"]}},"xrefs":[{"source":"ICD-10","code":"Q27.3","qualifier":"NTBT","icd_relation":"attributed","validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":715339,"name":"Multifocal peripheral venous malformation","classifications":[147,198]}],"children":[],"genes":[{"symbol":"TEK","name":"TEK receptor tyrosine kinase","gene_type":"gene with protein product","association":"Disease-causing somatic mutation(s) in","status":"Assessed","source":"19079259[PMID]","hgnc":"11724","ensembl":"ENSG00000120156","omim":"600221","loci":["9p21.2"]}],"genes_via_subtypes":[],"inheritance":["Not applicable"],"onset":["Childhood","Infancy","Neonatal"],"prevalence":[{"type":"Point prevalence","qualification":"Class only","class":"Unknown","value":0.0,"area":"Worldwide","status":"Validated","source":"ORPHANET"}],"phenotypes":null}