{"orpha":363294,"name":"Genetic syndromic Pierre Robin 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-363294/","orphanet_url":"https://www.orpha.net/en/disease/detail/363294","names":{"fr":{"name":"Syndrome de Pierre Robin syndromique d'origine génétique"},"de":{"name":"Pierre-Robin-Syndrom, syndromales, genetisch bedingtes"},"es":{"name":"Síndrome de Pierre Robin sindrómico de origen genético"},"it":{"name":"Sindrome di Pierre Robin sindromica genetica"},"nl":{"name":"Genetisch syndromaal syndroom van Pierre Robin"},"pt":{"name":"Síndrome de Pierre Robin sindromática genética"},"pl":{"name":"Syndromiczny zespół Pierre'a i Robina uwarunkowany genetycznie"},"cs":{"name":"Geneticky podmíněný syndromický Pierre Robinův syndrom"},"uk":{"name":"Генетично обумовлений синдром Пєра Робена"},"zh":{"name":"遗传性综合征性皮埃尔罗宾综合征"},"tr":{"name":"Genetik sendromik Pierre Robin sendromu"}},"xrefs":[{"source":"MONDO","code":"18187","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680982","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":728642,"name":"Genetic syndrome or malformation associated with head and neck malformations","classifications":[156]}],"children":[{"orpha":364577,"name":"Intellectual disability-brachydactyly-Pierre Robin syndrome","type":"Malformation syndrome"},{"orpha":138047,"name":"Pierre Robin syndrome associated with a chromosomal anomaly","type":"Category"},{"orpha":138055,"name":"Pierre Robin syndrome associated with bone disease","type":"Category"},{"orpha":138050,"name":"Pierre Robin syndrome associated with branchial archs anomalies","type":"Category"},{"orpha":138041,"name":"Pierre Robin syndrome associated with collagen disease","type":"Category"},{"orpha":2886,"name":"TARP syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}