{"orpha":600691,"name":"Combined deficiency of factor VII and factor X","type":"Disease","group":"Disorder","status":"active","flags":[],"synonyms":[],"definition":null,"note":null,"url":"https://raremap.alftech.space/d/ORPHA-600691/","orphanet_url":"https://www.orpha.net/en/disease/detail/600691","names":{"fr":{"name":"Déficit combiné en facteurs VII et X"},"de":{"name":"Faktor VII und Faktor X, kombinierter Mangel"},"es":{"name":"Deficiencia combinada de los factores VII y X"},"it":{"name":"Deficit combinato del fattore VII e X"},"nl":{"name":"Gecombineerde deficiëntie van factor VII en factor X"},"pt":{"name":"Deficiência de factor VII e factor X combinada"},"pl":{"name":"Złożony niedobór czynnika VII i X"},"cs":{"name":"Kombinovaný deficit faktoru VII a faktoru X"},"uk":{"name":"Комбінований дефіцит фактора VII та фактора X"}},"xrefs":[{"source":"ICD-10","code":"D68.2","qualifier":"NTBT","icd_relation":"attributed","validated":true},{"source":"ICD-11","code":"3B14.2","qualifier":"NTBT","icd_relation":"attributed","validated":true},{"source":"MONDO","code":"0035776","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681529","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97992,"name":"Rare hematologic disease"},"parents":[{"orpha":68334,"name":"Rare hemorrhagic disorder due to a constitutional coagulation factors defect","classifications":[156,194]}],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":["Adolescent","Adult","Childhood","Infancy","Neonatal"],"prevalence":[{"type":"Cases/families","qualification":"Case(s)","class":null,"value":7.0,"area":"Worldwide","status":"Validated","source":"28164683[PMID]"},{"type":"Point prevalence","qualification":"Class only","class":"<1 / 1 000 000","value":0.0,"area":"Worldwide","status":"Validated","source":"28164683[PMID]_ORPHANET"}],"phenotypes":null}