{"orpha":177907,"name":"Prader-Willi syndrome due to translocation","type":"Etiological subtype","group":"Subtype of disorder","status":"active","flags":[],"synonyms":[],"definition":null,"note":"This disease is described under Prader-Willi syndrome","url":"https://raremap.alftech.space/d/ORPHA-177907/","orphanet_url":"https://www.orpha.net/en/disease/detail/177907","names":{"fr":{"name":"Syndrome de Prader-Willi dû à une translocation"},"de":{"name":"Prader-Willi-Syndrom durch Translokation"},"es":{"name":"Síndrome de Prader-Willi por traslocación"},"it":{"name":"Sindrome di Prader-Willi da traslocazione"},"nl":{"name":"Prader-Willisyndroom door translocatie"},"pt":{"name":"Síndrome de Prader-Willi por translocação"},"pl":{"name":"Zespół Pradera i Willego spowodowany translokacją"},"cs":{"name":"Praderův-Williho syndrom na podkladě translokace","synonyms":["Prader-Williho syndrom na podkladě translokace"]},"uk":{"name":"Синдром Прадера-Віллі внаслідок транслокації"},"zh":{"name":"染色体易位所致Prader-Willi综合征"},"tr":{"name":"Translokasyona bağlı Prader-Willi sendromu"}},"xrefs":[{"source":"OMIM","code":"176270","qualifier":"NTBT","icd_relation":null,"validated":true},{"source":"ICD-10","code":"Q87.1","qualifier":"NTBT","icd_relation":"attributed","validated":true},{"source":"ICD-11","code":"LD90.3","qualifier":"NTBT","icd_relation":"attributed","validated":true,"icd11_uri":"null"},{"source":"MONDO","code":"0015785","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680509","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":739,"name":"Prader-Willi syndrome","classifications":[147,156,181,193,201,205]}],"children":[],"genes":[{"symbol":"SNRPN","name":"small nuclear ribonucleoprotein polypeptide N","gene_type":"gene with protein 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