{"orpha":263746,"name":"Y chromosome number 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-263746/","orphanet_url":"https://www.orpha.net/en/disease/detail/263746","names":{"fr":{"name":"Syndrome d'anomalie du nombre de chromosome y"},"de":{"name":"Chromosom Y-Anomalie, numerische"},"es":{"name":"Síndrome de anomalía numérica del cromosoma Y"},"it":{"name":"Sindrome anomalia numerica del cromosoma Y"},"nl":{"name":"Numerieke anomalie van Y-chromosoom-syndroom"},"pt":{"name":"Anomalia do número de cromossoma Y"},"pl":{"name":"Zespół aberracji liczbowej chromosomu Y"},"cs":{"name":"Anomálie počtu chromozomů Y"},"uk":{"name":"Аномалія кількості Y-хромосоми"},"zh":{"name":"Y染色体数目异常"},"tr":{"name":"Y kromozom sayısı anomalisi"}},"xrefs":[{"source":"ICD-11","code":"LD52","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"1632180154"},{"source":"MONDO","code":"17005","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C4736189","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":1772,"name":"45,X/46,XY mixed gonadal dysgenesis","type":"Malformation syndrome"},{"orpha":8,"name":"47,XYY syndrome","type":"Malformation syndrome"},{"orpha":99329,"name":"48,XYYY syndrome","type":"Malformation syndrome"},{"orpha":99330,"name":"49,XYYYY syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}