{"orpha":263723,"name":"Polysomy of X chromosome 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-263723/","orphanet_url":"https://www.orpha.net/en/disease/detail/263723","names":{"fr":{"name":"Syndrome de polysomie du chromosome x"},"de":{"name":"Chromosom X-Polysomie"},"es":{"name":"Síndrome de polisomía del cromosoma X"},"it":{"name":"Sindrome polisomia del cromosoma X"},"nl":{"name":"Polysomie van X chromosoom-syndroom"},"pt":{"name":"Polissomia do cromossoma X"},"pl":{"name":"Zespół polisomii chromosomu X"},"cs":{"name":"Polyzomie chromozomu X"},"uk":{"name":"Полісомія Х-хромосоми"},"zh":{"name":"X染色体多体"},"tr":{"name":"X kromozomunun polizomisi"}},"xrefs":[{"source":"MONDO","code":"17002","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680726","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":263717,"name":"X chromosome number anomaly with female phenotype syndrome","classifications":[147,156]}],"children":[{"orpha":11,"name":"Pentasomy X syndrome","type":"Malformation syndrome"},{"orpha":9,"name":"Tetrasomy X syndrome","type":"Malformation syndrome"},{"orpha":3375,"name":"Trisomy X syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}