{"orpha":325713,"name":"Genetic 46,XY difference of sex development of endocrine origin","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["Genetic 46,XY DSD of endocrine origin","Genetic 46,XY disorder of sex development of endocrine origin"],"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-325713/","orphanet_url":"https://www.orpha.net/en/disease/detail/325713","names":{"fr":{"name":"Différence du développement sexuel 46,XY d'origine endocrine et génétique","synonyms":["ADS 46,XY d'origine endocrine et génétique","Anomalie du développement sexuel 46,XY d'origine endocrine et génétique","DSD 46,XY d'origine endocrine et génétique"]},"de":{"name":"Störung der Geschlechtsentwicklung 46,XY, genetisch bedingte, endokrinen Ursprungs","synonyms":["46,XY-DSD, genetische Formen endokrinen Ursprungs"]},"es":{"name":"Desarrollo sexual diferente 46,XY genético de origen endocrino","synonyms":["DSD 46,XY genético de origen endocrino","Trastorno del desarrollo sexual 46,XY genético de origen endocrino"]},"it":{"name":"Disturbo genetico dello sviluppo sessuale 46,XY di origine endocrina","synonyms":["DSD 46,XY genetico di origine endocrina"]},"nl":{"name":"Genetische 46,XY-geslachtsontwikkelingsstoornis van endocriene oorsprong","synonyms":["Genetische 46,XY-DSD van endocriene oorsprong"]},"pt":{"name":"Doença do desenvolvimento sexual 46,XY genética de origem endócrina"},"pl":{"name":"Zaburzenie różnicowania płci z kariotypem 46,XY uwarunkowane genetycznie pochodzenia endokrynologicznego","synonyms":["ZRP 46,XY uwarunkowane genetycznie pochodzenia endokrynologicznego"]},"cs":{"name":"Geneticky podmíněná 46,XY porucha sexuálního vývoje endokrinního původu","synonyms":["Geneticky podmíněná 46,XY DSD endokrinního původu"]},"uk":{"name":"Генетичне порушення статевої диференціації 46,XУ ендокринного походження","synonyms":["Генетичне 46,XY порушення статевого розвитку ендокринного походження","Генетичне 46,XY ПСР ендокринного походження"]},"zh":{"name":"遗传性内分泌源性46，XY性发育障碍","synonyms":["遗传性内分泌源性46，XYDSD"]},"tr":{"name":"Endokrin kökenli genetik 46, XY cinsiyet gelişim bozukluğu","synonyms":["Endokrin kaynaklı genetik 46,XY DSD"]}},"xrefs":[{"source":"UMLS","code":"C5679862","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":325706,"name":"Genetic 46,XY difference of sex development","classifications":[156]}],"children":[{"orpha":325357,"name":"46,XY difference of sex development due to impaired androgen production","type":"Category"},{"orpha":754,"name":"Androgen insensitivity syndrome","type":"Clinical group"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}