{"orpha":715466,"name":"Syndromic low resistance capillary malformation","type":"Clinical group","group":"Group of disorders","status":"active","flags":[],"synonyms":["Syndromic capillary malformation with fast-flow"],"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-715466/","orphanet_url":"https://www.orpha.net/en/disease/detail/715466","names":{"fr":{"name":"Malformation capillaire à faible résistance syndromique","synonyms":["Malformation capillaire syndromique à flux rapide"]},"de":{"name":"Syndromale kapilläre schnell-fließende Fehlbildung","synonyms":["Syndromale kapilläre fast-flow Malformation"]},"es":{"name":"Malformación capilar sindrómica de baja resistencia","synonyms":["Malformación capilar sindrómica de alto flujo"]},"it":{"name":"Malformazione capillare sindromica a bassa resistenza","synonyms":["Malformazione capillare sindromica a flusso rapido"]},"nl":{"name":"Syndromale capillaire malformatie met lage weerstand","synonyms":["Syndromale fast-flow capillaire malformatie","Syndromale capillaire malformatie met snelle bloedstroom"]},"pt":{"name":"Syndromes with capillary malformation with fast-flow as a major feature"},"pl":{"name":"Syndromiczna malformacja naczyń włosowatych o niskim oporze","synonyms":["Syndromic capillary malformation with fast-flow"]},"cs":{"name":"Syndromic low resistance capillary malformation","synonyms":["Syndromic capillary malformation with fast-flow"]}},"xrefs":[],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98028,"name":"Rare circulatory system disease"},"parents":[{"orpha":715463,"name":"Low resistance capillary malformation","classifications":[147,198]}],"children":[{"orpha":137667,"name":"Capillary malformation-arteriovenous malformation","type":"Clinical group"},{"orpha":90307,"name":"Parkes Weber syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}