{"orpha":180148,"name":"Syndromic uterovaginal malformation","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"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-180148/","orphanet_url":"https://www.orpha.net/en/disease/detail/180148","names":{"fr":{"name":"Malformation utéro-vaginale syndromique"},"de":{"name":"Uterovaginale Fehlbildung, syndromale"},"es":{"name":"Malformación uterovaginal sindrómica"},"it":{"name":"Malformazione uterovaginale sindromica"},"nl":{"name":"Syndromale uterovaginale malformatie"},"pt":{"name":"Malformação uterovaginal sindromática"},"pl":{"name":"Syndromiczna malformacja macicy i pochwy"},"cs":{"name":"Syndromické malformace dělohy a pochvy"},"uk":{"name":"Синдромальна матково-вагінальна вада розвитку"},"zh":{"name":"综合征性子宫阴道畸形"},"tr":{"name":"Sendromik uterovajinal malformasyon"}},"xrefs":[{"source":"MONDO","code":"15846","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680492","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":180062,"name":"Uterovaginal malformation","classifications":[205]}],"children":[{"orpha":2973,"name":"46,XX difference of sex development-anorectal anomalies syndrome","type":"Malformation syndrome"},{"orpha":1552,"name":"Currarino syndrome","type":"Malformation syndrome"},{"orpha":3411,"name":"Double uterus-hemivagina-renal agenesis syndrome","type":"Malformation syndrome"},{"orpha":2438,"name":"Hand-foot-genital syndrome","type":"Malformation syndrome"},{"orpha":3097,"name":"Meacham syndrome","type":"Malformation syndrome"},{"orpha":2491,"name":"Müllerian duct anomalies-limb anomalies syndrome","type":"Malformation syndrome"},{"orpha":991,"name":"PAGOD syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}