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

36376006: Congenital absence of esophagus (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2005. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
60705011 Congenital absence of esophagus en Synonym Active Entire term case insensitive SNOMED CT core module
486432019 Congenital absence of oesophagus en Synonym Active Entire term case insensitive SNOMED CT core module
768121017 Congenital absence of esophagus (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1216503015 Absent oesophagus en Synonym Active Entire term case insensitive SNOMED CT core module
1217993011 Absent esophagus en Synonym Active Entire term case insensitive SNOMED CT core module


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital absence of esophagus Is a Congenital anomaly of esophagus true Inferred relationship Existential restriction modifier
Congenital absence of esophagus Is a Congenital absence of alimentary tract false Inferred relationship Existential restriction modifier
Congenital absence of esophagus Finding site Esophageal structure true Inferred relationship Existential restriction modifier 1
Congenital absence of esophagus Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 1
Congenital absence of esophagus Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Congenital absence of esophagus Occurrence Congenital false Inferred relationship Existential restriction modifier
Congenital absence of esophagus Occurrence Congenital false Inferred relationship Existential restriction modifier
Congenital absence of esophagus Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 1
Congenital absence of esophagus Finding site Esophageal structure false Inferred relationship Existential restriction modifier 1
Congenital absence of esophagus Is a Congenital malformation of upper alimentary tract false Inferred relationship Existential restriction modifier
Congenital absence of esophagus Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Congenital absence of esophagus Finding site Esophageal structure false Inferred relationship Existential restriction modifier 2
Congenital absence of esophagus Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 2
Congenital absence of esophagus Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital absence of esophagus Is a Congenital partial absence of alimentary tract true Inferred relationship Existential restriction modifier
Congenital absence of esophagus Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Congenital absence of esophagus Associated morphology Agenesis false Inferred relationship Existential restriction modifier 1
Congenital absence of esophagus Finding site Entire esophagus false Inferred relationship Existential restriction modifier 1
Congenital absence of esophagus Associated morphology Absence true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital absence of esophagus with tracheoesophageal fistula Is a False Congenital absence of esophagus Inferred relationship Existential restriction modifier
Agenesis of esophagus Is a True Congenital absence of esophagus Inferred relationship Existential restriction modifier

This concept is not in any reference sets

Back to Start