{"orpha":182117,"name":"Non-syndromic urogenital tract malformation of female","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-182117/","orphanet_url":"https://www.orpha.net/en/disease/detail/182117","names":{"fr":{"name":"Malformation urogénitale non syndromique de la femme"},"de":{"name":"Urogenitale Fehlbildungen, weibliche, nichtsyndromale Formen"},"es":{"name":"Malformación no sindrómica del tracto urogenital femenino"},"it":{"name":"Malformazione non sindromica dell'apparato urogenitale femminile"},"nl":{"name":"Niet-syndromale malformatie van urogenitaal systeem van vrouw"},"pt":{"name":"Malformação do trato genito-urinário feminino não sindromática"},"pl":{"name":"Niesyndromiczna malformacja żeńskiego układu moczowo-płciowego"},"cs":{"name":"Nesyndromické malformace urogenitálního traktu žen"},"uk":{"name":"Несиндромальна вада розвитку урогенітального тракту у жінок"},"zh":{"name":"女性非综合征性泌尿生殖道畸形"},"tr":{"name":"Kadınlarda non-endromik ürogenital sistem malformasyonu"}},"xrefs":[{"source":"MONDO","code":"15932","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680592","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":165704,"name":"Non-syndromic urogenital tract malformation","classifications":[147,185,233]}],"children":[{"orpha":603515,"name":"Isolated female hypospadias","type":"Morphological anomaly"},{"orpha":647794,"name":"Isolated persistent urogenital sinus","type":"Morphological anomaly"},{"orpha":180065,"name":"Non-syndromic uterovaginal malformation","type":"Category"},{"orpha":180151,"name":"Rare vaginal malformation","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}