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66865009: Congenital duplication of esophagus (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
111068012 Congenital duplication of esophagus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
500545018 Congenital duplication of oesophagus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
806525019 Congenital duplication of esophagus (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3028081017 Oesophageal duplication en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3028150012 Esophageal duplication en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
111068012 Congenital duplication of esophagus en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
111068012 Congenital duplication of esophagus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
500545018 Congenital duplication of oesophagus en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
500545018 Congenital duplication of oesophagus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
806525019 Congenital duplication of esophagus (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
806525019 Congenital duplication of esophagus (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3028081017 Oesophageal duplication en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3028081017 Oesophageal duplication en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3028150012 Esophageal duplication en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3028150012 Esophageal duplication en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3411051001000116 Ösophagus-Verdoppelung de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4608811000241114 duplication congénital de l'oesophage fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4608811000241114 duplication congénital de l'oesophage fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3411051001000116 Ösophagus-Verdoppelung de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital duplication of esophagus (disorder) Is a Congenital anomaly of esophagus true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of esophagus (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of esophagus (disorder) Finding site Oesophageal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of esophagus (disorder) Finding site Digestive organ structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of esophagus (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of esophagus (disorder) Associated morphology Double structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of esophagus (disorder) Finding site Entire digestive tract including mouth, oesophagus, stomach and intestines false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of esophagus (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of esophagus (disorder) Is a Congenital duplication of digestive organs true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of esophagus (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of esophagus (disorder) Associated morphology Double structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of esophagus (disorder) Finding site Oesophageal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of esophagus (disorder) Is a Congenital malformation of upper alimentary tract false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of esophagus (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital duplication of esophagus (disorder) Finding site Oesophageal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital duplication of esophagus (disorder) Associated morphology Double structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital duplication of esophagus (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of esophagus (disorder) 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
Congenital tubular duplication of esophagus Is a True Congenital duplication of esophagus (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Duplication cyst of esophagus (disorder) Is a True Congenital duplication of esophagus (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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