{"orpha":138050,"name":"Pierre Robin syndrome associated with branchial archs anomalies","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["Pierre Robin sequence associated with branchial archs anomalies"],"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-138050/","orphanet_url":"https://www.orpha.net/en/disease/detail/138050","names":{"fr":{"name":"Syndrome de Pierre Robin associée à une anomalie des arcs branchiaux","synonyms":["Séquence de Pierre Robin associée à une anomalie des arcs branchiaux"]},"de":{"name":"Pierre-Robin-Sequenz mit assoziierter Kiemenbogen-Fehlbildung","synonyms":["Pierre-Robin-Syndrom - Kiemenbogendefekt"]},"es":{"name":"Síndrome de Pierre Robin asociado con anomalías de los arcos branquiales","synonyms":["Secuencia de Pierre Robin asociada con anomalías de los arcos branquiales"]},"it":{"name":"Sindrome di Pierre Robin associata a anomalie degli archi branchiali","synonyms":["Sequenza di Pierre Robin associata a anomalie degli archi branchiali"]},"nl":{"name":"Syndroom van Pierre Robin geassocieerd met kieuwbooganomalieën","synonyms":["Pierre Robin sequentie geassocieerd met kieuwbooganomalieën"]},"pt":{"name":"Sequência de Pierre Robin associada a anomalia dos arcos branquiais"},"pl":{"name":"Zespół Pierre'a Robina związany z anomaliami łuków skrzelowych","synonyms":["Sekwencja Pierre'a Robina związana z anomaliami łuków skrzelowych"]},"cs":{"name":"Pierre Robinův syndrom spojený s anomáliemi branchiálních oblouků","synonyms":["Pierre Robinova sekvence spojená s anomáliemi branchiálních oblouků"]},"uk":{"name":"Синдром Пєра Робена, повязаний з аномаліями бранхіальних гілок","synonyms":["Послідовність Пєра Робена повязана з аномаліями гілкових дуг"]},"zh":{"name":"鳃弓异常相关Pierre-Robin综合征","synonyms":["Pierre-Robin序列征相关鳃弓畸形"]},"tr":{"name":"Brankial ark anomalileri ilişkili Pierre Robin sendromu","synonyms":["Branşel kemer anomalileri ile ilişkili Pierre Robin dizisi"]}},"xrefs":[{"source":"UMLS","code":"C5679602","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"19897","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":363294,"name":"Genetic syndromic Pierre Robin syndrome","classifications":[156]},{"orpha":138044,"name":"Rare disease with Pierre Robin syndrome","classifications":[147,200,209]}],"children":[{"orpha":245,"name":"Nager syndrome","type":"Malformation syndrome"},{"orpha":861,"name":"Treacher-Collins syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}