Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Nov 2024. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2606010 | Congenital stenosis of esophagus | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
509350018 | Congenital stenosis of oesophagus | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
2744042010 | Congenital stenosis of esophagus (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5406335013 | Congenital esophageal stenosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5406336014 | Congenital oesophageal stenosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital stenosis of esophagus | Is a | Lesion of oesophagus | true | Inferred relationship | Some | ||
Congenital stenosis of esophagus | Is a | Congenital anomaly of esophagus | true | Inferred relationship | Some | ||
Congenital stenosis of esophagus | Is a | Gastrointestinal stenosis | true | Inferred relationship | Some | ||
Congenital stenosis of esophagus | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital stenosis of esophagus | Associated morphology | Stenosis (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
Congenital stenosis of esophagus | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Congenital stenosis of esophagus | Finding site | Oesophageal structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
A rare non-syndromic oesophageal malformation characterised by intrinsic narrowing of the oesophagus, caused by congenital malformation of oesophageal wall architecture present at birth. Patients manifest dysphagia and progressive vomiting. Oesophageal food impaction, failure to thrive or respiratory distress can be present. Symptoms are often attributed to colic or reflux, thus diagnosis is often difficult. | Is a | True | Congenital stenosis of esophagus | Inferred relationship | Some | |
Congenital cardiospasm | Is a | True | Congenital stenosis of esophagus | Inferred relationship | Some | |
Congenital tracheoesophageal fistula with esophageal stenosis (disorder) | Is a | True | Congenital stenosis of esophagus | Inferred relationship | Some |
This concept is not in any reference sets