{"orpha":156249,"name":"Larynx anomaly","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-156249/","orphanet_url":"https://www.orpha.net/en/disease/detail/156249","names":{"fr":{"name":"Anomalie du larynx"},"de":{"name":"Larynx-Anomalie"},"es":{"name":"Anomalía laríngea"},"it":{"name":"Anomalia della laringe"},"nl":{"name":"Larynxanomalie"},"pt":{"name":"Anomalia da laringe"},"pl":{"name":"Wada gardła"},"cs":{"name":"Anomálie laryngu"},"uk":{"name":"Аномалія гортані"},"zh":{"name":"喉畸形"},"tr":{"name":"Gırtlak anomalisi"}},"xrefs":[{"source":"ICD-10","code":"Q31","qualifier":"E","icd_relation":"specific","validated":true},{"source":"ICD-11","code":"LA71","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"2041437327"},{"source":"MONDO","code":"15504","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":96333,"name":"Rare otorhinolaryngological malformation","classifications":[147,200]}],"children":[{"orpha":137935,"name":"Airway infantile hemangioma","type":"Disease"},{"orpha":141124,"name":"Congenital laryngeal cyst","type":"Morphological anomaly"},{"orpha":137932,"name":"Congenital laryngeal palsy","type":"Malformation syndrome"},{"orpha":2373,"name":"Congenital laryngomalacia","type":"Malformation syndrome"},{"orpha":141121,"name":"Congenital subglottic stenosis","type":"Malformation syndrome"},{"orpha":2291,"name":"Congenital velopharyngeal incompetence","type":"Morphological anomaly"},{"orpha":2374,"name":"Isolated congenital laryngeal web","type":"Malformation syndrome"},{"orpha":2808,"name":"Laryngeal abductor paralysis","type":"Malformation syndrome"},{"orpha":2372,"name":"Laryngocele","type":"Malformation syndrome"},{"orpha":2004,"name":"Laryngotracheoesophageal cleft","type":"Morphological anomaly"},{"orpha":1202,"name":"Larynx atresia","type":"Malformation syndrome"},{"orpha":137926,"name":"Primary laryngeal lymphangioma","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}