Status: current, Not 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 |
| 5406339019 | Non-syndromic congenital stenosis of esophagus | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5406340017 | Non syndromic congenital oesophageal stenosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5406341018 | Non-syndromic congenital stenosis of esophagus (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5406342013 | Non syndromic congenital esophageal stenosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5406343015 | Non-syndromic congenital stenosis of oesophagus | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5406344014 | 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. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5406345010 | A rare non-syndromic esophageal malformation characterized by intrinsic narrowing of the esophagus, caused by congenital malformation of esophageal wall architecture present at birth. Patients manifest dysphagia and progressive vomiting. Esophageal food impaction, failure to thrive or respiratory distress can be present. Symptoms are often attributed to colic or reflux, thus diagnosis is often difficult. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Non-syndromic congenital stenosis of esophagus | Is a | Congenital stenosis of esophagus | true | Inferred relationship | Some | ||
| Non-syndromic congenital stenosis of esophagus | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Non-syndromic congenital stenosis of esophagus | Finding site | Oesophageal structure | true | Inferred relationship | Some | 1 | |
| Non-syndromic congenital stenosis of esophagus | Associated morphology | Stenosis (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Non-syndromic congenital stenosis of esophagus | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR