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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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital upper esophageal web Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital upper esophageal web survenue (attribut) congénital true Inferred relationship Some 1
Congenital upper esophageal web localisation d'une constatation (attribut) tiers supérieur de l'œsophage (structure corporelle) true Inferred relationship Some 1
Congenital upper esophageal web morphologie associée (attribut) Congenital webbing true Inferred relationship Some 1
Congenital upper esophageal web est un(e) (attribut) Congenital web of esophagus true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Canada English language reference set (foundation metadata concept)

GB English

US English

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