{"orpha":165704,"name":"Non-syndromic urogenital tract 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-165704/","orphanet_url":"https://www.orpha.net/en/disease/detail/165704","names":{"fr":{"name":"Malformation urogénitale non syndromique"},"de":{"name":"Fehlbildung des Urogenitaltraktes, nicht-syndromale"},"es":{"name":"Malformación no sindrómica del tracto urogenital"},"it":{"name":"Malformazione non sindromica del tratto urogenitale"},"nl":{"name":"Niet-syndromale urogenitale kanaalmalformatie"},"pt":{"name":"Malformação do trato urogenital não-sindromática"},"pl":{"name":"Niesyndromiczna malformacja układu moczowo-płciowego"},"cs":{"name":"Nesyndromické malformace urogenitálního traktu"},"uk":{"name":"Несиндромні вади розвитку урогенітального тракту"},"zh":{"name":"非综合征性泌尿生殖道畸形"},"tr":{"name":"Sendromik olmayan ürogenital sistem malformasyonu"}},"xrefs":[{"source":"MONDO","code":"15619","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680443","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":506213,"name":"Rare disorder potentially indicated for kidney transplant","classifications":[233]},{"orpha":83001,"name":"Urogenital tract malformation","classifications":[147,185]}],"children":[{"orpha":182117,"name":"Non-syndromic urogenital tract malformation of female","type":"Category"},{"orpha":182121,"name":"Non-syndromic urogenital tract malformation of male","type":"Category"},{"orpha":182124,"name":"Non-syndromic urogenital tract malformation of male and female","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}