{"orpha":400003,"name":"Rare genetic disorder with obstructive azoospermia","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["Rare genetic disorder due to impaired sperm transport"],"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-400003/","orphanet_url":"https://www.orpha.net/en/disease/detail/400003","names":{"fr":{"name":"Maladie génétique rare avec azoospermie obstructive","synonyms":["Maladie génétique rare avec azoospermie excrétoire"]},"de":{"name":"Seltene genetische Störung mit obstruktiver Azoospermie","synonyms":["Seltene genetische Störung durch Beeinträchtigung des Spermientransportes"]},"es":{"name":"Trastorno genético raro con azoospermia obstructiva","synonyms":["Trastorno genético raro por un defecto en el transporte del esperma"]},"it":{"name":"Disturbo genetico raro con azoospermia ostruttiva","synonyms":["Disturbo genetico raro da difetto nel trasporto dello sperma"]},"nl":{"name":"Zeldzame genetische aandoening met obstructieve azoöspermie","synonyms":["Zeldzame genetische aandoening door storing van spermatransport"]},"pt":{"name":"Doença genética rara com azoospermia obstrutiva"},"pl":{"name":"Rzadkie genetyczne zaburzenie z azoospermią obstrukcyjną","synonyms":["Rzadkie genetyczne zaburzenie z powodu upośledzonego transportu spermy"]},"cs":{"name":"Vzácné geneticky podmíněné poruchy s obstrukční azoospermií","synonyms":["Vzácné geneticky podmíněné poruchy s porušeným transportem spermií"]},"uk":{"name":"Рідкісне генетично обумовлене захворювання з обструктивною азооспермією","synonyms":["Рідкісне генетичне захворювання, повязане з порушенням транспортування сперматозоїдів"]},"zh":{"name":"罕见遗传性障碍伴梗阻性无精症","synonyms":["精子运输障碍所致罕见遗传性障碍"]},"tr":{"name":"Obstrüktif azospermi ile seyreden genetik bozukluk","synonyms":["Bozulmuş sperm taşınmasına bağlı nadir görülen genetik bozukluk"]}},"xrefs":[{"source":"MONDO","code":"18409","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680007","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98047,"name":"Rare infertility"},"parents":[{"orpha":399998,"name":"Male infertility due to obstructive azoospermia of genetic origin","classifications":[156]}],"children":[{"orpha":730,"name":"Autosomal dominant polycystic kidney disease","type":"Disease"},{"orpha":731,"name":"Autosomal recessive polycystic kidney disease","type":"Disease"},{"orpha":586,"name":"Cystic fibrosis","type":"Disease"},{"orpha":2856,"name":"Persistent Müllerian duct syndrome","type":"Malformation syndrome"},{"orpha":3471,"name":"Young syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}