{"orpha":280205,"name":"Laryngotracheoesophageal cleft type 0","type":"Clinical subtype","group":"Subtype of disorder","status":"active","flags":[],"synonyms":["LTEC0","Laryngo-tracheo-esophageal cleft type 0"],"definition":"Laryngo-tracheo-esophageal cleft (LC) type 0 is a congenital respiratory tract anomaly characterized by a submucosal laryngo-tracheo-esophageal cleft with minor symptoms or an asymptomatic course.","note":null,"url":"https://raremap.alftech.space/d/ORPHA-280205/","orphanet_url":"https://www.orpha.net/en/disease/detail/280205","names":{"fr":{"name":"Fente laryngo-trachéo-oesophagienne type 0","synonyms":["LTEC0"],"definition":"La fente laryngo-trachéo-oesophagienne (FLTO) de type 0 est une anomalie congénitale de l'appareil respiratoire, caractérisée par une fente laryngo-trachéo-oesophagienne sous muqueuse asymptomatique ou à l'origine d'une symptomatologie mineure."},"de":{"name":"Laryngo-tracheo-ösophageale Spalte Typ 0","synonyms":["LTEC0"],"definition":"Die Laryngo-tracheo-ösophageal-Spalte (LC) Typ 0 ist eine kongenitale Anomalie der Atemwege und gekennzeichnet durch eine submuköse laryngo-tracheo-ösophageale Spalte, die nur geringe Symptome verursacht oder symptomlos bleibt."},"es":{"name":"Hendidura laringotraqueoesofágica tipo 0","synonyms":["Hendidura laringo-traqueo-esofágica tipo 0","LTEC0"],"definition":"La hendidura laringo-traqueo-esofágica (HLTE) tipo 0 es una anomalía congénita del tracto respiratorio caracterizada por una hendidura laringo-traqueo-esofágica submucosa con síntomas menores o un curso asintomático."},"it":{"name":"Schisi laringo-tracheo-esofagea, tipo 0","synonyms":["LTEC0"],"definition":"La schisi laringo-tracheo-esofagea (LC) tipo 0 è un'anomalia congenita delle vie respiratorie caratterizzata da schisi laringo-tracheo-esofagea sottomucosa associata a sintomi minori o a un decorso asintomatico."},"nl":{"name":"Laryngo-tracheo-oesofageale fissuur type 0","synonyms":["LTEC0"],"definition":"Laryngo-tracheo-oesofageale fissuur (LC) type 0 is een aangeboren afwijking van de luchtwegen gekenmerkt door een submucosale laryngo-tracheo-oesofageale fissuur met geringe symptomen of een asymptomatisch verloop."},"pt":{"name":"Fenda laringo-traqueo-esofágica tipo 0","synonyms":["LTECO"],"definition":"A fenda laringo-traqueo-esofágica (LC) tipo 0 é uma anomalia congénita do trato respiratório caracterizada por uma fenda laringo-traqueo-esofágica submucosa com sintomas ligeiros ou curso assintomático."},"pl":{"name":"Szczelina krtaniowo-tchawiczo-przełykowa typu 0","synonyms":["LTEC0"]},"cs":{"name":"Laryngotracheoezofageální rozštěp, typ 0","synonyms":["LTEC0"]},"uk":{"name":"Ларинготрахеостравохідна розщілина, тип 0","synonyms":["Ларинго-трахео-стравохідна щілина 0 типу","LTEC0"],"definition":"Laryngo-tracheo-esophageal cleft (LC) type 0 is a congenital respiratory tract anomaly characterized by a submucosal laryngo-tracheo-esophageal cleft with minor symptoms or an asymptomatic course."},"zh":{"name":"喉气管食道裂0型","synonyms":["0型喉-气管-食道裂"],"definition":"喉-气管-食管裂（LC）0型是一种先天性呼吸道畸形，其特征是黏膜下喉气管食管裂，症状较轻或无症状。"},"tr":{"name":"Laringotrakeoözofageal yarık tip 0","synonyms":["LTEC0","Laringo-trakeo-özofageal yarık tip 0"]}},"xrefs":[{"source":"ICD-10","code":"Q32.1","qualifier":"NTBT","icd_relation":"attributed","validated":true},{"source":"ICD-11","code":"LA72","qualifier":"NTBT","icd_relation":"index","validated":true,"icd11_uri":"1007234149"},{"source":"MONDO","code":"0017220","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5438977","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":2004,"name":"Laryngotracheoesophageal cleft","classifications":[147,156,182,184,186,200]}],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[{"type":"Point prevalence","qualification":"Class only","class":"Unknown","value":0.0,"area":"Worldwide","status":"Not yet validated","source":"ORPHANET"}],"phenotypes":null}