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840510006: Congenital absence of epiglottis (disorder)


Status: current, Defined. Date: 31-Jul 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3902188017 Congenital absence of epiglottis (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3902189013 Congenital absence of epiglottis en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital absence of epiglottis Is a Congenital anomaly of larynx true Inferred relationship Some
Congenital absence of epiglottis Is a Absence of larynx true Inferred relationship Some
Congenital absence of epiglottis Is a Disorder of epiglottis true Inferred relationship Some
Congenital absence of epiglottis Finding site Epiglottis structure true Inferred relationship Some 1
Congenital absence of epiglottis Occurrence Congenital true Inferred relationship Some 1
Congenital absence of epiglottis Pathological process Pathological developmental process true Inferred relationship Some 1
Congenital absence of epiglottis Associated morphology Congenital absence false Inferred relationship Some 1
Congenital absence of epiglottis Associated morphology Absence true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Respiratory finding reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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