FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

716280004: Congenital tubular duplication of esophagus (disorder)


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


0 descendants.

Expanded Value Set


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)

Back to Start