{"orpha":435609,"name":"Genetic 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-435609/","orphanet_url":"https://www.orpha.net/en/disease/detail/435609","names":{"fr":{"name":"Anomalie du larynx d'origine génétique"},"de":{"name":"Larynx-Anomalie, genetisch bedingte"},"es":{"name":"Anomalía laríngea genética"},"it":{"name":"Anomalia genetica della laringe"},"nl":{"name":"Genetische anomalie van larynx"},"pt":{"name":"Anomalia da laringe genética"},"pl":{"name":"Genetyczna wada krtani"},"cs":{"name":"Geneticky podmíněná anomálie laryngu"},"uk":{"name":"Генетично обумовлена аномалія гортані"},"zh":{"name":"遗传性喉异常"},"tr":{"name":"Genetik gırtlak anomalisi"}},"xrefs":[{"source":"UMLS","code":"C5681173","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":435603,"name":"Genetic otorhinolaryngological malformation","classifications":[156]}],"children":[{"orpha":2373,"name":"Congenital laryngomalacia","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":1202,"name":"Larynx atresia","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}