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770619007: Congenital upper esophageal web (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3701622017 Congenital upper esophageal web en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3701623010 Congenital upper esophageal web (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3701624016 Congenital upper oesophageal web en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3701622017 Congenital upper esophageal web en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3701623010 Congenital upper esophageal web (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3701624016 Congenital upper oesophageal web en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5905981000241113 membrane congénitale de l'œsophage supérieur fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5905981000241113 membrane congénitale de l'œsophage supérieur fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital upper esophageal web (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital upper esophageal web (disorder) Finding site Structure of upper third of oesophagus true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital upper esophageal web (disorder) Associated morphology Congenital webbing true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital upper esophageal web (disorder) Is a Congenital web of esophagus true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital upper esophageal web (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

This concept is not in any reference sets

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