Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Jun 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5068187017 | Congenital laryngotracheoesophageal cleft | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5068188010 | Congenital laryngotracheoesophageal cleft (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5068189019 | Congenital laryngotracheo-oesophageal cleft | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5068191010 | LTEC - laryngo-tracheo-esophageal cleft | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5068192015 | LTEC - laryngo-tracheo-oesophageal cleft | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5068194019 | A congenital malformation characterized by an abnormal posterior sagittal communication between the larynx and the pharynx, possibly extending downward between the trachea and the esophagus. Five types of laryngo-tracheo-esophageal cleft have been described based on the downward extension of the cleft. The disorder is often associated with other congenital abnormalities. Laryngeal clefts result from failure of fusion of the posterior cricoid lamina and abnormal development of the tracheo-esophageal septum. The disorder appears to be mostly sporadic although some familial cases with suspected autosomal dominant transmission have been reported. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5068195018 | A congenital malformation characterised by an abnormal posterior sagittal communication between the larynx and the pharynx, possibly extending downward between the trachea and the oesophagus. Five types of laryngo-tracheo-oesophageal cleft have been described based on the downward extension of the cleft. The disorder is often associated with other congenital abnormalities. Laryngeal clefts result from failure of fusion of the posterior cricoid lamina and abnormal development of the tracheo-oesophageal septum. The disorder appears to be mostly sporadic although some familial cases with suspected autosomal dominant transmission have been reported. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Laryngeal cleft type I | est un(e) (attribut) | True | Congenital laryngotracheoesophageal cleft | Inferred relationship | Some | |
Laryngeal cleft type II | est un(e) (attribut) | True | Congenital laryngotracheoesophageal cleft | Inferred relationship | Some | |
Laryngeal cleft type III | est un(e) (attribut) | True | Congenital laryngotracheoesophageal cleft | Inferred relationship | Some | |
Laryngeal cleft type IV | est un(e) (attribut) | True | Congenital laryngotracheoesophageal cleft | Inferred relationship | Some | |
Laryngeal cleft type 0 | est un(e) (attribut) | True | Congenital laryngotracheoesophageal cleft | Inferred relationship | Some |
This concept is not in any reference sets