{"orpha":263749,"name":"X and Y chromosomal anomaly syndrome","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-263749/","orphanet_url":"https://www.orpha.net/en/disease/detail/263749","names":{"fr":{"name":"Syndrome d'anomalie des chromosomes x et y"},"de":{"name":"Chromosom Y und X-Anomalie"},"es":{"name":"Síndrome de anomalía cromosómica X e Y"},"it":{"name":"Sindrome anomalia dei cromosomi X e Y"},"nl":{"name":"Anomalie van X- en Y-chromosoom-syndroom"},"pt":{"name":"Anomalia cromossómica X e Y"},"pl":{"name":"Zespół aberracji chromosomów X i Y"},"cs":{"name":"Anomálie X a Y chromozomu"},"uk":{"name":"Хромосомна аномалія X та Y хромосом"},"zh":{"name":"X和Y染色体异常"},"tr":{"name":"X ve Y kromozom anomalisi"}},"xrefs":[{"source":"MONDO","code":"17006","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680725","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":98156,"name":"Sex-chromosome number anomaly syndrome","classifications":[147,156]}],"children":[{"orpha":10,"name":"48,XXYY syndrome","type":"Malformation syndrome"},{"orpha":261534,"name":"49,XXXYY syndrome","type":"Malformation syndrome"},{"orpha":199310,"name":"Tetragametic chimerism syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}