{"orpha":98158,"name":"Chromosome Y structural 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-98158/","orphanet_url":"https://www.orpha.net/en/disease/detail/98158","names":{"fr":{"name":"Syndrome d'anomalie de structure du chromosome y"},"de":{"name":"Chromosom Y mit Strukturanomalität"},"es":{"name":"Síndrome de anomalía estructural del cromosoma Y"},"it":{"name":"Anomalia strutturale del cromosoma Y"},"nl":{"name":"Chromosoom Y structurele anomalie-syndroom"},"pt":{"name":"Anomalia estrutural do cromossoma Y"},"pl":{"name":"Zespół aberracji strukturalnych chromosomu Y"},"cs":{"name":"Strukturní aberace chromozomu Y"},"uk":{"name":"Структурна аномалія хромосоми Y"},"zh":{"name":"Y染色体结构异常"},"tr":{"name":"Kromozom Y yapısal anomalisi"}},"xrefs":[{"source":"ICD-10","code":"Q98.6","qualifier":"E","icd_relation":"specific","validated":true},{"source":"ICD-11","code":"LD53","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"1096926039"},{"source":"UMLS","code":"C4736190","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":98157,"name":"Sex-chromosome structural anomaly syndrome","classifications":[147,156]}],"children":[{"orpha":1646,"name":"Chromosome Y microdeletion syndrome","type":"Malformation syndrome"},{"orpha":96325,"name":"Isochromosome Y syndrome","type":"Category"},{"orpha":261529,"name":"Ring chromosome Y syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}