{"orpha":435603,"name":"Genetic 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-435603/","orphanet_url":"https://www.orpha.net/en/disease/detail/435603","names":{"fr":{"name":"Malformation otorhinolaryngologique d'origine génétique"},"de":{"name":"Otorhinolaryngologische Fehlbildung, genetisch bedingte"},"es":{"name":"Malformación otorrinolaringológica genética"},"it":{"name":"Malformazione genetica d'interesse otorinolaringoiatrico"},"nl":{"name":"Genetische otorinolaryngologische malformatie"},"pt":{"name":"Malformação otorrinolaringológica genética"},"pl":{"name":"Malformacja otorynolaryngologiczna uwarunkowana genetycznie"},"cs":{"name":"Geneticky podmíněné otorinolaryngologické malformace"},"uk":{"name":"Генетично обумовлена оториноларингологічна вада розвитку"},"zh":{"name":"遗传性耳鼻喉科畸形"},"tr":{"name":"Genetik kulak burun boğaz malformasyonu"}},"xrefs":[{"source":"MONDO","code":"18562","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681175","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":183583,"name":"Genetic head and neck malformation","classifications":[156]},{"orpha":466084,"name":"Genetic otorhinolaryngologic disease","classifications":[156]}],"children":[{"orpha":435609,"name":"Genetic larynx anomaly","type":"Category"},{"orpha":435606,"name":"Genetic nose and cavum anomaly","type":"Category"},{"orpha":435612,"name":"Genetic tracheal anomaly","type":"Category"},{"orpha":156243,"name":"Pinnae and external auditory canal anomaly","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}