FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

11266002: Upper esophageal web (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
19521014 Upper esophageal web en Synonym Active Entire term case insensitive SNOMED CT core module
195359016 Upper oesophageal web en Synonym Active Entire term case insensitive SNOMED CT core module
375073013 Cricopharyngeal web en Synonym Active Entire term case insensitive SNOMED CT core module
375074019 Postcricoid web en Synonym Active Entire term case insensitive SNOMED CT core module
375075018 Hypopharyngeal web en Synonym Active Entire term case insensitive SNOMED CT core module
375076017 PC - Postcricoid web en Synonym Active Entire term case sensitive SNOMED CT core module
375077014 Postcricoid oesophageal web en Synonym Active Entire term case insensitive SNOMED CT core module
375078016 Postcricoid esophageal web en Synonym Active Entire term case insensitive SNOMED CT core module
642342013 Upper esophageal web (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Upper esophageal web Is a Disorder of hypopharynx false Inferred relationship Existential restriction modifier
Upper esophageal web Is a Esophageal web true Inferred relationship Existential restriction modifier
Upper esophageal web Finding site Structure of postcricoid region false Inferred relationship Existential restriction modifier
Upper esophageal web Associated morphology Congenital webbing false Inferred relationship Existential restriction modifier
Upper esophageal web Finding site Esophageal structure false Inferred relationship Existential restriction modifier 2
Upper esophageal web Associated morphology Acquired web false Inferred relationship Existential restriction modifier 1
Upper esophageal web Finding site Structure of upper third of esophagus false Inferred relationship Existential restriction modifier 1
Upper esophageal web Is a Disorder of neck false Inferred relationship Existential restriction modifier
Upper esophageal web Is a Ear, nose and throat disorder false Inferred relationship Existential restriction modifier
Upper esophageal web Is a Disorder of respiratory system false Inferred relationship Existential restriction modifier
Upper esophageal web Is a Disorder of hypopharynx false Inferred relationship Existential restriction modifier
Upper esophageal web Is a Congenital malformation false Inferred relationship Existential restriction modifier
Upper esophageal web Occurrence Congenital false Inferred relationship Existential restriction modifier
Upper esophageal web Is a Congenital disease false Inferred relationship Existential restriction modifier
Upper esophageal web Associated morphology Acquired web false Inferred relationship Existential restriction modifier 1
Upper esophageal web Finding site Structure of upper third of esophagus true Inferred relationship Existential restriction modifier 1
Upper esophageal web Is a Lesion of esophagus false Inferred relationship Existential restriction modifier
Upper esophageal web Occurrence Period of life beginning after birth and ending before death true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Plummer-Vinson syndrome Is a False Upper esophageal web Inferred relationship Existential restriction modifier

This concept is not in any reference sets

Back to Start