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770619007: Congenital upper esophageal web (disorder)


Status: current, Defined. Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3701622017 Congenital upper esophageal web en Synonym Active Case insensitive SNOMED CT core
3701623010 Congenital upper esophageal web (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3701624016 Congenital upper oesophageal web en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital upper oesophageal web Pathological process Pathological developmental process true Inferred relationship Some 1
Congenital upper oesophageal web Occurrence Congenital true Inferred relationship Some 1
Congenital upper oesophageal web Finding site Structure of upper third of oesophagus true Inferred relationship Some 1
Congenital upper oesophageal web Associated morphology Congenital webbing true Inferred relationship Some 1
Congenital upper oesophageal web Is a Congenital web of oesophagus true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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