{"orpha":68335,"name":"Rare chromosomal anomaly","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-68335/","orphanet_url":"https://www.orpha.net/en/disease/detail/68335","names":{"fr":{"name":"Anomalie chromosomique rare"},"de":{"name":"Seltene Chromosomenanomalie"},"es":{"name":"Anomalías cromosómicas raras"},"it":{"name":"Anomalia cromosomica"},"nl":{"name":"Zeldzame chromosomale anomalie"},"pt":{"name":"Anomalia cromossómica rara"},"pl":{"name":"Zaburzenia chromosomowe"},"cs":{"name":"Anomálie chromozomů"},"uk":{"name":"Рідкісна хромосомна аномалія"},"zh":{"name":"罕见染色体异常"},"tr":{"name":"Nadir kromozom anomalisi"}},"xrefs":[{"source":"MONDO","code":"19040","qualifier":"E","icd_relation":null,"validated":true},{"source":"MeSH","code":"D002869","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681313","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":93890,"name":"Rare developmental defect during embryogenesis","classifications":[147]},{"orpha":98053,"name":"Rare genetic disease","classifications":[156]}],"children":[{"orpha":98127,"name":"Autosomal anomaly syndrome","type":"Category"},{"orpha":1052,"name":"Mosaic variegated aneuploidy syndrome","type":"Malformation syndrome"},{"orpha":96321,"name":"Polyploidy syndrome","type":"Category"},{"orpha":98155,"name":"Sex-chromosome anomaly syndrome","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}