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721154006: Congenital chalasia of esophagus (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3324469016 Congenital chalasia of esophagus (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3324470015 Congenital chalasia of esophagus en Synonym Active Entire term case insensitive SNOMED CT core module
3324471016 Congenital chalasia of oesophagus en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital chalasia of esophagus Is a Congenital disease true Inferred relationship Existential restriction modifier
Congenital chalasia of esophagus Is a Chalasia of lower esophageal sphincter true Inferred relationship Existential restriction modifier
Congenital chalasia of esophagus Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital chalasia of esophagus Finding site Inferior esophageal sphincter structure true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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