FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.24  |  FHIR Version n/a  User: [n/a]

770619007: Congenital upper esophageal web (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3701622017 Congenital upper esophageal web en Synonym Active Entire term case insensitive SNOMED CT core module
3701623010 Congenital upper esophageal web (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3701624016 Congenital upper oesophageal web 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 upper esophageal web Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital upper esophageal web Finding site Structure of upper third of esophagus true Inferred relationship Existential restriction modifier 1
Congenital upper esophageal web Associated morphology Congenital webbing true Inferred relationship Existential restriction modifier 1
Congenital upper esophageal web Is a Congenital web of esophagus true Inferred relationship Existential restriction modifier
Congenital upper esophageal web Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start