{"orpha":83001,"name":"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-83001/","orphanet_url":"https://www.orpha.net/en/disease/detail/83001","names":{"fr":{"name":"Malformation urogénitale"},"de":{"name":"Urogenitale Fehlbildungen"},"es":{"name":"Malformación del tracto urogenital"},"it":{"name":"Malformazione del tratto urogenitale"},"nl":{"name":"Urogenitaal kanaalmalformatie"},"pt":{"name":"Malformação do trato urogenital"},"pl":{"name":"Malformacje układu moczowo-płciowego"},"cs":{"name":"Malformace urogenitálního traktu"},"uk":{"name":"Вади розвитку сечостатевих шляхів"},"zh":{"name":"泌尿生殖道畸形"},"tr":{"name":"Ürogenital sistem malformasyonu"}},"xrefs":[{"source":"MONDO","code":"0019356","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"19356","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0042063","qualifier":"E","icd_relation":null,"validated":true},{"source":"MedDRA","code":"10062334","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":93890,"name":"Rare developmental defect during embryogenesis","classifications":[147]},{"orpha":101433,"name":"Rare urogenital disease","classifications":[185]}],"children":[{"orpha":165704,"name":"Non-syndromic urogenital tract malformation","type":"Category"},{"orpha":165707,"name":"Syndromic urogenital tract malformation","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}