{"orpha":138059,"name":"Teratogenic Pierre Robin syndrome","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["Teratogenic Pierre Robin sequence"],"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-138059/","orphanet_url":"https://www.orpha.net/en/disease/detail/138059","names":{"fr":{"name":"Syndrome de Pierre Robin d'origine tératogène","synonyms":["Séquence de Pierre Robin d'origine tératogène"]},"de":{"name":"Pierre-Robin-Sequenz, teratogene","synonyms":["Pierre-Robin-Syndrom durch teratogene Substanzen"]},"es":{"name":"Síndrome de Pierre Robin teratogénico","synonyms":["Secuencia de Pierre Robin teratogénica"]},"it":{"name":"Sindrome teratogenica di Pierre Robin","synonyms":["Sequenza teratogenica di Pierre Robin"]},"nl":{"name":"Teratogeen syndroom van Pierre Robin","synonyms":["Teratogene Pierre Robin sequentie"]},"pt":{"name":"Sequência de Pierre Robin teratogénica"},"pl":{"name":"Teratogenny zespół Pierre' a Robina","synonyms":["Teratogenna sekwencja Pierre' a Robina"]},"cs":{"name":"Pierre Robinův syndrom způsobený teratogeny","synonyms":["Teratogenní Pierre Robinova sekvence","Pierre Robinova sekvence způsobená teratogeny"]},"uk":{"name":"Тератогенний синдром Пєра Робена","synonyms":["Тератогенна послідовність Пєра Робіна"]},"zh":{"name":"致畸性Pierre Robin综合征","synonyms":["致畸性Pierre-Robin序列征"]},"tr":{"name":"Teratojenik Pierre Robin sendromu","synonyms":["Teratojenik Pierre Robin dizisi"]}},"xrefs":[{"source":"MONDO","code":"15323","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5679603","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"19899","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":138044,"name":"Rare disease with Pierre Robin syndrome","classifications":[147,200,209]}],"children":[{"orpha":1908,"name":"Aminopterin/methotrexate embryofetopathy","type":"Malformation syndrome"},{"orpha":1911,"name":"Cocaine embryofetopathy","type":"Malformation syndrome"},{"orpha":1926,"name":"Diabetic embryopathy","type":"Malformation syndrome"},{"orpha":1915,"name":"Fetal alcohol syndrome","type":"Malformation syndrome"},{"orpha":1912,"name":"Fetal hydantoin syndrome","type":"Malformation syndrome"},{"orpha":1910,"name":"Fetal iodine syndrome","type":"Malformation syndrome"},{"orpha":1917,"name":"Fetal methylmercury syndrome","type":"Malformation syndrome"},{"orpha":1918,"name":"Fetal minoxidil syndrome","type":"Malformation syndrome"},{"orpha":295,"name":"Fetal parvovirus syndrome","type":"Malformation syndrome"},{"orpha":1913,"name":"Fetal trimethadione syndrome","type":"Malformation syndrome"},{"orpha":1906,"name":"Fetal valproate spectrum disorder","type":"Malformation syndrome"},{"orpha":1909,"name":"Indomethacin embryofetopathy","type":"Malformation syndrome"},{"orpha":2305,"name":"Isotretinoin syndrome","type":"Malformation syndrome"},{"orpha":2216,"name":"Maternal hyperthermia-induced birth defects","type":"Malformation syndrome"},{"orpha":2209,"name":"Maternal phenylketonuria syndrome","type":"Malformation syndrome"},{"orpha":1923,"name":"Methimazole embryofetopathy","type":"Malformation syndrome"},{"orpha":1919,"name":"Phenobarbital embryopathy","type":"Malformation syndrome"},{"orpha":485358,"name":"Propylthiouracil embryofetopathy","type":"Malformation syndrome"},{"orpha":1920,"name":"Toluene embryopathy","type":"Malformation syndrome"},{"orpha":1914,"name":"Vitamin K antagonist embryofetopathy","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}