{"orpha":98155,"name":"Sex-chromosome anomaly syndrome","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["Allosome anomaly"],"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-98155/","orphanet_url":"https://www.orpha.net/en/disease/detail/98155","names":{"fr":{"name":"Syndrome d'anomalies des gonosomes","synonyms":["Anomalies des chromosomes sexuels"]},"de":{"name":"Gonosomen-Anomalie","synonyms":["Anomalie der Geschlechtschromosomen"]},"es":{"name":"Síndrome de anomalía gonosómica","synonyms":["Anomalías en los cromosomas sexuales"]},"it":{"name":"Sindrome anomalia dei cromosomi sessuali","synonyms":["Anomalia dei cromosomi sessuali"]},"nl":{"name":"Gonosomenanomalie-syndroom","synonyms":["Geslachtschromosomenanomalie"]},"pt":{"name":"Anomalia dos gonossomas"},"pl":{"name":"Zespół aberracji chromosomów płciowych","synonyms":["Anomalia chromosmów płci"]},"cs":{"name":"Aberace gonozomů","synonyms":["Aberace pohlavních chromozomů"]},"uk":{"name":"Аномалія статевих хромосом","synonyms":["Аномалія алосом"]},"zh":{"name":"性染色体异常","synonyms":["异染色体异常"]},"tr":{"name":"Cinsiyet kromozomu anomalisi","synonyms":["Allozom anomalisi"]}},"xrefs":[{"source":"MONDO","code":"0020058","qualifier":"E","icd_relation":null,"validated":true},{"source":"MeSH","code":"D012729","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0036868","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":68335,"name":"Rare chromosomal anomaly","classifications":[147,156]}],"children":[{"orpha":98156,"name":"Sex-chromosome number anomaly syndrome","type":"Category"},{"orpha":98157,"name":"Sex-chromosome structural anomaly syndrome","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}