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1230239009: Congenital laryngotracheoesophageal cleft (disorder)


Status: current, Primitive. Date: 30-Jun 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5068187017 Congenital laryngotracheoesophageal cleft en Synonym Active Case insensitive SNOMED CT core
5068188010 Congenital laryngotracheoesophageal cleft (disorder) en Fully specified name Active Case insensitive SNOMED CT core
5068189019 Congenital laryngotracheo-oesophageal cleft en Synonym Active Case insensitive SNOMED CT core
5068191010 LTEC - laryngo-tracheo-esophageal cleft en Synonym Active Case sensitive SNOMED CT core
5068192015 LTEC - laryngo-tracheo-oesophageal cleft en Synonym Active Case sensitive 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 Case sensitive 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 Case sensitive SNOMED CT core


5 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital laryngotracheo-oesophageal cleft Occurrence Congenital true Inferred relationship Some 1
Congenital laryngotracheo-oesophageal cleft Associated morphology Developmental failure of fusion true Inferred relationship Some 1
Congenital laryngotracheo-oesophageal cleft Pathological process Pathological developmental process true Inferred relationship Some 1
Congenital laryngotracheo-oesophageal cleft Occurrence Congenital true Inferred relationship Some 2
Congenital laryngotracheo-oesophageal cleft Finding site Laryngeal structure true Inferred relationship Some 2
Congenital laryngotracheo-oesophageal cleft Associated morphology Abnormal communication true Inferred relationship Some 2
Congenital laryngotracheo-oesophageal cleft Pathological process Pathological developmental process true Inferred relationship Some 2
Congenital laryngotracheo-oesophageal cleft Is a Congenital cleft of posterior cricoid cartilage true Inferred relationship Some
Congenital laryngotracheo-oesophageal cleft Finding site Structure of lamina of cricoid cartilage true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Laryngeal cleft type I Is a True Congenital laryngotracheo-oesophageal cleft Inferred relationship Some
Laryngeal cleft type II Is a True Congenital laryngotracheo-oesophageal cleft Inferred relationship Some
Laryngeal cleft type III Is a True Congenital laryngotracheo-oesophageal cleft Inferred relationship Some
Laryngeal cleft type IV Is a True Congenital laryngotracheo-oesophageal cleft Inferred relationship Some
Submucosal laryngeal cleft Is a True Congenital laryngotracheo-oesophageal cleft Inferred relationship Some

Reference Sets

Clinical finding foundation reference set

Respiratory finding reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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