{"orpha":138044,"name":"Rare disease with 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-138044/","orphanet_url":"https://www.orpha.net/en/disease/detail/138044","names":{"fr":{"name":"Maladie rare avec syndrome de Pierre Robin"},"de":{"name":"Seltene Krankheit mit Pierre Robin-Syndrom","synonyms":["Pierre-Robin-Syndrom, syndromales"]},"es":{"name":"Enfermedad rara con síndrome de Pierre Robin"},"it":{"name":"Malattia rara con sindrome di Pierre Robin"},"nl":{"name":"Zeldzame ziekte met syndroom van Pierre Robin"},"pt":{"name":"Sequência de Pierre Robin, sindrómica"},"pl":{"name":"Rzadka choroba z zespołem Pierre'a Robina"},"cs":{"name":"Vzácná onemocnění s Pierre Robinovým syndromem"},"uk":{"name":"Рідкісне захворювання з синдромом Пєра Робена"},"zh":{"name":"伴皮埃尔-罗宾综合征的罕见病"},"tr":{"name":"Pierre Robin sendromu ile seyreden nadir hastalık"}},"xrefs":[{"source":"MONDO","code":"15319","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680627","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"19895","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":138063,"name":"OBSOLETE: Syndrome associated with Pierre Robin syndrome","status":"inactive"},{"type":"Referred to","orpha":138066,"name":"OBSOLETE: Pierre Robin syndrome associated with miscellaneous anomalies","status":"inactive"}],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":156237,"name":"Syndrome or malformation associated with head and neck malformations","classifications":[147,200,209]}],"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"},{"orpha":138059,"name":"Teratogenic Pierre Robin syndrome","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[{"type":"Prevalence at birth","qualification":"Class only","class":"Unknown","value":0.0,"area":"Worldwide","status":"Not yet validated","source":"24433508[PMID]"},{"type":"Point prevalence","qualification":"Class only","class":"Unknown","value":0.0,"area":"Europe","status":"Not yet validated","source":"ORPHANET"}],"phenotypes":null}