{"orpha":156622,"name":"Genetic 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-156622/","orphanet_url":"https://www.orpha.net/en/disease/detail/156622","names":{"fr":{"name":"Malformation urogénitale génétique"},"de":{"name":"Harnwegsfehlbildung, genetisch bedingte"},"es":{"name":"Malformación genética del tracto urogenital"},"it":{"name":"Malformazione genetica del tratto urogenitale"},"nl":{"name":"Genetische urogenitaal kanaalmalformatie"},"pt":{"name":"Malformação do trato urogenital, genética"},"pl":{"name":"Wady genetyczne układu moczowo-płciowego"},"cs":{"name":"Geneticky podmíněné malformace urogenitální traktu"},"uk":{"name":"Генетичні вади розвитку сечостатевої системи"},"zh":{"name":"遗传性泌尿生殖道畸形"},"tr":{"name":"Genetik ürogenital sistem malformasyonu"}},"xrefs":[{"source":"UMLS","code":"C5680640","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":156619,"name":"Rare genetic urogenital disease","classifications":[156]}],"children":[{"orpha":48,"name":"Congenital bilateral absence of vas deferens","type":"Morphological anomaly"},{"orpha":289365,"name":"Familial vesicoureteral reflux","type":"Malformation syndrome"},{"orpha":73217,"name":"Müllerian aplasia","type":"Clinical group"},{"orpha":95706,"name":"Non-syndromic posterior hypospadias","type":"Morphological anomaly"},{"orpha":165707,"name":"Syndromic urogenital tract malformation","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}