{"orpha":96333,"name":"Rare otorhinolaryngological malformation","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-96333/","orphanet_url":"https://www.orpha.net/en/disease/detail/96333","names":{"fr":{"name":"Malformation otorhinolaryngologique rare"},"de":{"name":"Otorhinolaryngologische Fehlbildung, seltene"},"es":{"name":"Malformación otorrinolaringológica rara"},"it":{"name":"Malformazione rara d'interesse otorinolaringoiatrico"},"nl":{"name":"Zeldzame otorinolaryngologische malformatie"},"pt":{"name":"Malformação otorrinolaringológica, rara"},"pl":{"name":"Rzadka malformacja uszno-nosowo-krtaniowa"},"cs":{"name":"Vzácné otorinolaryngologické malformace","synonyms":["Vzácné ORL malformace"]},"uk":{"name":"Рідкісна оториноларингологічна вада розвитку"},"zh":{"name":"罕见耳鼻喉畸形"},"tr":{"name":"Nadir kulak burun boğaz malformasyonu"}},"xrefs":[{"source":"UMLS","code":"C5681539","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":155832,"name":"Rare head and neck malformation","classifications":[147]},{"orpha":98036,"name":"Rare otorhinolaryngologic disease","classifications":[200]}],"children":[{"orpha":155835,"name":"Cysts and fistulae of the face and oral cavity","type":"Category"},{"orpha":156249,"name":"Larynx anomaly","type":"Category"},{"orpha":164004,"name":"Middle and/or inner ear anomaly","type":"Category"},{"orpha":156246,"name":"Nose and cavum anomaly","type":"Category"},{"orpha":155896,"name":"Otomandibular dysplasia","type":"Category"},{"orpha":156243,"name":"Pinnae and external auditory canal anomaly","type":"Category"},{"orpha":156252,"name":"Tracheal anomaly","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}