Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3305379017 | Congenital tubular duplication of esophagus (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3305380019 | Congenital tubular duplication of esophagus | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3305381015 | Congenital tubular duplication of oesophagus | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5401295010 | A rare, non-syndromic, congenital esophageal malformation characterized by a second structure with individual lumen and stratified squamous mucosa and muscularis mucosa lying within or adjacent to the true esophagus causing dysphagia, nausea, vomiting, retrosternal pain and respiratory problems (stridor and recurrent pneumonia) and usually presenting in childhood. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401296011 | A rare, non-syndromic, congenital oesophageal malformation characterised by a second structure with individual lumen and stratified squamous mucosa and muscularis mucosa lying within or adjacent to the true oesophagus causing dysphagia, nausea, vomiting, retrosternal pain and respiratory problems (stridor and recurrent pneumonia) and usually presenting in childhood. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3305379017 | Congenital tubular duplication of esophagus (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3305379017 | Congenital tubular duplication of esophagus (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3305380019 | Congenital tubular duplication of esophagus | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3305380019 | Congenital tubular duplication of esophagus | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3305381015 | Congenital tubular duplication of oesophagus | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3305381015 | Congenital tubular duplication of oesophagus | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3305382010 | Tubular duplication of the esophagus is a rare congenital malformation where a second structure with individual lumen and stratified squamous mucosa and muscularis mucosa lies within or adjacent to the true esophagus causing dysphagia, nausea, vomiting, retrosternal pain and respiratory problems (stridor and recurrent pneumonia) and usually presenting in children. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3305383017 | Tubular duplication of the oesophagus is a rare congenital malformation where a second structure with individual lumen and stratified squamous mucosa and muscularis mucosa lies within or adjacent to the true oesophagus causing dysphagia, nausea, vomiting, retrosternal pain and respiratory problems (stridor and recurrent pneumonia) and usually presenting in children. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401295010 | A rare, non-syndromic, congenital esophageal malformation characterized by a second structure with individual lumen and stratified squamous mucosa and muscularis mucosa lying within or adjacent to the true esophagus causing dysphagia, nausea, vomiting, retrosternal pain and respiratory problems (stridor and recurrent pneumonia) and usually presenting in childhood. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401296011 | A rare, non-syndromic, congenital oesophageal malformation characterised by a second structure with individual lumen and stratified squamous mucosa and muscularis mucosa lying within or adjacent to the true oesophagus causing dysphagia, nausea, vomiting, retrosternal pain and respiratory problems (stridor and recurrent pneumonia) and usually presenting in childhood. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3410211001000118 | Tubuläre Ösophagus-Duplikation | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
5875431000241118 | duplication tubulaire congénitale de l'œsophage | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
5875431000241118 | duplication tubulaire congénitale de l'œsophage | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3410211001000118 | Tubuläre Ösophagus-Duplikation | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital tubular duplication of esophagus | Is a | Congenital duplication of esophagus (disorder) | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Congenital tubular duplication of esophagus | Associated morphology | Double structure | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
Congenital tubular duplication of esophagus | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
Congenital tubular duplication of esophagus | Finding site | Esophageal part | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
Congenital tubular duplication of esophagus | Pathological process (attribute) | Pathological developmental process (qualifier value) | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)