{"orpha":156619,"name":"Rare genetic urogenital disease","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-156619/","orphanet_url":"https://www.orpha.net/en/disease/detail/156619","names":{"fr":{"name":"Maladie urogénitale génétique rare"},"de":{"name":"Urogenitale Anomalie, genetisch bedingte"},"es":{"name":"Anomalías urogenitales genéticas raras"},"it":{"name":"Anomalia urogenitale genetica"},"nl":{"name":"Zeldzame genetische urogenitale ziekte"},"pt":{"name":"Anomalia urogenital genética"},"pl":{"name":"Rzadka genetyczna choroba układu moczowo-płciowego"},"cs":{"name":"Vzácné geneticky podmíněné nemoci urogenitálního traktu"},"uk":{"name":"Рідкісне генетично обумовлене урогенітальне захворювання"},"zh":{"name":"罕见的遗传性泌尿生殖疾病"},"tr":{"name":"Nadir genetik ürogenital hastalık"}},"xrefs":[{"source":"MONDO","code":"15511","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680641","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":101433,"name":"Rare urogenital disease"},"parents":[{"orpha":98053,"name":"Rare genetic disease","classifications":[156]}],"children":[{"orpha":325690,"name":"Genetic difference of sex development","type":"Category"},{"orpha":156622,"name":"Genetic urogenital tract malformation","type":"Category"},{"orpha":404463,"name":"Multisystemic smooth muscle dysfunction syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}