{"orpha":180065,"name":"Non-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-180065/","orphanet_url":"https://www.orpha.net/en/disease/detail/180065","names":{"fr":{"name":"Malformation utérovaginale non syndromique"},"de":{"name":"Uterovaginale Fehlbildung, nicht-syndromale"},"es":{"name":"Malformación uterovaginal no sindrómica"},"it":{"name":"Malformazione uterovaginale non sindromica"},"nl":{"name":"Niet-syndromale uterovaginale malformatie"},"pt":{"name":"Malformação uterovaginal não-sindromática"},"pl":{"name":"Niesyndromiczna wada macicy i pochwy"},"cs":{"name":"Nesyndromické malformace dělohy a pochvy"},"uk":{"name":"Несиндромальна матково-вагінальна вада розвитку"},"zh":{"name":"非综合征性子宫阴道畸形"},"tr":{"name":"Sendromik olmayan uterovajinal malformasyon"}},"xrefs":[{"source":"MONDO","code":"15829","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680487","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":182117,"name":"Non-syndromic urogenital tract malformation of female","classifications":[147,185,233]},{"orpha":180062,"name":"Uterovaginal malformation","classifications":[205]}],"children":[{"orpha":180142,"name":"Absence of uterine body","type":"Morphological anomaly"},{"orpha":180134,"name":"Bicornuate uterus","type":"Clinical group"},{"orpha":1916,"name":"Diethylstilbestrol syndrome","type":"Malformation syndrome"},{"orpha":73217,"name":"Müllerian aplasia","type":"Clinical group"},{"orpha":180122,"name":"Septate uterus","type":"Clinical group"},{"orpha":180145,"name":"Uterine cervical aplasia and agenesis","type":"Morphological anomaly"},{"orpha":180139,"name":"Uterine hypoplasia","type":"Morphological anomaly"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}