{"orpha":675359,"name":"Anastomosing hemangioma","type":"Disease","group":"Disorder","status":"active","flags":[],"synonyms":["Anastomosing haemangioma"],"definition":null,"note":null,"url":"https://raremap.alftech.space/d/ORPHA-675359/","orphanet_url":"https://www.orpha.net/en/disease/detail/675359","names":{"fr":{"name":"Hémangiome anastomotique"},"de":{"name":"Hämangiom, anastomosierendes"},"es":{"name":"Hemangioma anastomosante"},"it":{"name":"Emangioma anastomizzante"},"nl":{"name":"Anastomoserend hemangioom"},"pt":{"name":"Hemangioma anastomosante"},"pl":{"name":"Naczyniak zespalający","synonyms":["Anastomosing haemangioma"]},"cs":{"name":"Anastomozující hemangiom","synonyms":["Anastomosing haemangioma"]},"uk":{"name":"Анастомозуюча гемангіома"}},"xrefs":[{"source":"ICD-10","code":"D18.0","qualifier":"NTBT","icd_relation":"attributed","validated":true},{"source":"ICD-11","code":"2E81.0Y","qualifier":"NTBT","icd_relation":"attributed","validated":true},{"source":"MONDO","code":"0975757","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"975757","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C4329301","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":250908,"name":"Rare neoplastic disease"},"parents":[{"orpha":673470,"name":"Benign vascular tumor","classifications":[147,198,202]},{"orpha":459543,"name":"Rare genetic vascular tumor","classifications":[156]}],"children":[],"genes":[{"symbol":"GNA11","name":"G protein subunit alpha 11","gene_type":"gene with protein product","association":"Disease-causing somatic mutation(s) in","status":"Assessed","source":"31189994[PMID]","hgnc":"4379","ensembl":"ENSG00000088256","omim":"139313","loci":["19p13.3"]},{"symbol":"GNA14","name":"G protein subunit alpha 14","gene_type":"gene with protein product","association":"Disease-causing somatic mutation(s) in","status":"Assessed","source":"29574926[PMID]","hgnc":"4382","ensembl":"ENSG00000156049","omim":"604397","loci":["9q21.2"]},{"symbol":"GNAQ","name":"G protein subunit alpha q","gene_type":"gene with protein product","association":"Disease-causing somatic mutation(s) in","status":"Assessed","source":"28084343[PMID]","hgnc":"4390","ensembl":"ENSG00000156052","omim":"600998","loci":["9q21.2"]}],"genes_via_subtypes":[],"inheritance":["Not applicable"],"onset":["Adolescent","Adult","Elderly","Infancy"],"prevalence":[{"type":"Cases/families","qualification":"Case(s)","class":null,"value":32.0,"area":"Worldwide","status":"Validated","source":"26960722[PMID]"},{"type":"Point prevalence","qualification":"Class only","class":"<1 / 1 000 000","value":0.0,"area":"Worldwide","status":"Validated","source":"26960722[PMID]_ORPHANET"}],"phenotypes":null}