{"orpha":2005,"name":"OBSOLETE: Laryngo-tracheo-esophageal cleft-pulmonary hypoplasia syndrome","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: Novak syndrome"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Laryngotracheoesophageal cleft type 4","url":"https://raremap.alftech.space/d/ORPHA-2005/","orphanet_url":"https://www.orpha.net/en/disease/detail/2005","names":{"fr":{"name":"OBSOLETE : Syndrome de fente laryngo-trachéo-oesophagienne-hypoplasie pulmonaire","synonyms":["OBSOLETE : Syndrome de Novak"]},"de":{"name":"OBSOLET: Laryngo-tracheo-ösophageale Spalte-Pulmonale Hypoplasie-Syndrom"},"es":{"name":"OBSOLETO: Síndrome de hendidura laringotraqueoesofágica-hipoplasia pulmonar","synonyms":["OBSOLETO: Síndrome de Novak"]},"it":{"name":"OBSOLETO: Sindrome schisi laringo-tracheo-esofagea-ipoplasia polmonare","synonyms":["OBSOLETO: Sindrome di Novak"]},"nl":{"name":"OBSOLEET: Laryngo-tracheo-oesofageale spleet - pulmonale hypoplasie-syndroom","synonyms":["OBSOLEET: Syndroom van Novak"]},"pt":{"name":"OBSOLETO: Síndrome de fenda laringo-traqueo-esofágica-hipoplasia pulmonar"},"pl":{"name":"NIEAKTUALNE: Rozszczep krtaniowo-tchawiczo-przelykowy - hipoplazja pluc","synonyms":["NIEAKTUALNE: Zespół Novaka"]},"cs":{"name":"NEAKTUÁLNÍ: Laryngotracheoezofageální píštěl s plicní hypoplázií","synonyms":["NEAKTUÁLNÍ: Novakův syndrom"]},"uk":{"name":"ЗАСТАРІЛО: Синдром ларинго-трахео-стравохідної розщілини та легеневої гіпоплазії","synonyms":["ЗАСТАРІЛО: Синдром Новака"]},"zh":{"name":"弃用：喉-气管-食管裂口-肺发育不良综合征","synonyms":["Novak综合征"]},"tr":{"name":"Eski adı: Laringo-trakeo-özofagus yarık-pulmoner hipoplazi sendromu","synonyms":["Novak sendromu"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":93941,"name":"Laryngotracheoesophageal cleft type 4"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}