{"orpha":98159,"name":"Chromosome X 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-98159/","orphanet_url":"https://www.orpha.net/en/disease/detail/98159","names":{"fr":{"name":"Syndrome d'anomalie de structure du chromosome x"},"de":{"name":"Chromosom X mit Strukturanomalität"},"es":{"name":"Síndrome de anomalía estructural del cromosoma X"},"it":{"name":"Sindrome anomalia strutturale del cromosoma X"},"nl":{"name":"Chromosoom X structurele anomalie-syndroom"},"pt":{"name":"Anomalia estrutural do cromossoma X"},"pl":{"name":"Zespół aberracji strukturalnych chromosomu X"},"cs":{"name":"Strukturní aberace chromozomu X"},"uk":{"name":"Структурна аномалія хромосоми Х"},"zh":{"name":"X染色体结构异常"},"tr":{"name":"Kromozom X yapısal anomalisi"}},"xrefs":[{"source":"UMLS","code":"C5681501","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":263726,"name":"Partial deletion of chromosome X syndrome","type":"Category"},{"orpha":263768,"name":"Partial duplication of chromosome X syndrome","type":"Category"},{"orpha":263793,"name":"Uniparental disomy of chromosome X syndrome","type":"Category"},{"orpha":96201,"name":"X small rings syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}