{"orpha":183622,"name":"Genetic respiratory 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-183622/","orphanet_url":"https://www.orpha.net/en/disease/detail/183622","names":{"fr":{"name":"Malformation de l'appareil respiratorire d'origine génétique"},"de":{"name":"Fehlbildung des respiratorischen Systems, genetisch bedingte"},"es":{"name":"Malformación genética del aparato respiratorio"},"it":{"name":"Malformazione genetica dellapparato respiratorio"},"nl":{"name":"Genetische respiratoire malformatie"},"pt":{"name":"Malformação respiratória genética"},"pl":{"name":"Wada układu oddechowego uwarunkowana genetycznie"},"cs":{"name":"Geneticky podmíněné malformace dýchací soustavy"},"uk":{"name":"Генетично обумовлена респіраторна вада розвитку"},"zh":{"name":"遗传性呼吸系统多发畸形"},"tr":{"name":"Genetik solunum bozuklukları"}},"xrefs":[{"source":"UMLS","code":"C5680541","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":156610,"name":"Rare genetic respiratory disease","classifications":[156]}],"children":[{"orpha":1928,"name":"Congenital lobar emphysema","type":"Morphological anomaly"},{"orpha":3035,"name":"Growth delay-hydrocephaly-lung hypoplasia syndrome","type":"Malformation syndrome"},{"orpha":774,"name":"Hereditary hemorrhagic telangiectasia","type":"Disease"},{"orpha":2407,"name":"Laryngo-onycho-cutaneous syndrome","type":"Disease"},{"orpha":1120,"name":"Lung agenesis-heart defect-thumb anomalies syndrome","type":"Malformation syndrome"},{"orpha":2470,"name":"Matthew-Wood syndrome","type":"Malformation syndrome"},{"orpha":2257,"name":"Primary pulmonary hypoplasia","type":"Morphological anomaly"},{"orpha":3317,"name":"Thoracolaryngopelvic dysplasia","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}