{"orpha":325055,"name":"46,XX disorder of gonadal development","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-325055/","orphanet_url":"https://www.orpha.net/en/disease/detail/325055","names":{"fr":{"name":"Anomalie du développement des gonades 46,XX"},"de":{"name":"46,XX Störung der Gonadenentwicklung"},"es":{"name":"Anomalía del desarrollo gonadal 46,XX","synonyms":["Trastorno del desarrollo gonadal 46,XX"]},"it":{"name":"Disturbo dello sviluppo gonadico 46,XX"},"nl":{"name":"46,XX stoornis van gonadale ontwikkeling"},"pt":{"name":"Alteração 46, XX do desenvolvimento gonadal"},"pl":{"name":"Zaburzenie rozwoju gonad z kariotypem 46,XX"},"cs":{"name":"46,XX porucha pohlavního vývoje"},"uk":{"name":"46,XX порушення розвитку гонад"},"zh":{"name":"46，XX性腺发育不全"},"tr":{"name":"46, XX gonadal gelişim bozukluğu"}},"xrefs":[{"source":"MONDO","code":"17961","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680950","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":2982,"name":"46,XX difference of sex development","classifications":[147,185,193]},{"orpha":325697,"name":"Genetic 46,XX difference of sex development","classifications":[156]}],"children":[{"orpha":243,"name":"46,XX gonadal dysgenesis","type":"Malformation syndrome"},{"orpha":444048,"name":"46,XX ovarian dysgenesis-short stature syndrome","type":"Disease"},{"orpha":2138,"name":"46,XX ovotesticular difference of sex development","type":"Malformation syndrome"},{"orpha":393,"name":"46,XX testicular difference of sex development","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}