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1230239009: Congenital laryngotracheoesophageal cleft (disorder)


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


5 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital laryngotracheoesophageal cleft survenue (attribut) congénital true Inferred relationship Some 1
Congenital laryngotracheoesophageal cleft morphologie associée (attribut) Developmental failure of fusion (morphologic abnormality) true Inferred relationship Some 1
Congenital laryngotracheoesophageal cleft Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital laryngotracheoesophageal cleft survenue (attribut) congénital true Inferred relationship Some 2
Congenital laryngotracheoesophageal cleft localisation d'une constatation (attribut) larynx (structure corporelle) true Inferred relationship Some 2
Congenital laryngotracheoesophageal cleft morphologie associée (attribut) Abnormal communication true Inferred relationship Some 2
Congenital laryngotracheoesophageal cleft Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Congenital laryngotracheoesophageal cleft est un(e) (attribut) Congenital cleft of posterior cricoid cartilage true Inferred relationship Some
Congenital laryngotracheoesophageal cleft localisation d'une constatation (attribut) Structure of lamina of cricoid cartilage true Inferred relationship Some 1

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

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