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840510006: Congenital absence of epiglottis (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2020. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3902188017 Congenital absence of epiglottis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3902189013 Congenital absence of epiglottis 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 absence of epiglottis Is a Congenital anomaly of larynx true Inferred relationship Existential restriction modifier
Congenital absence of epiglottis Is a Absence of larynx true Inferred relationship Existential restriction modifier
Congenital absence of epiglottis Is a Disorder of epiglottis true Inferred relationship Existential restriction modifier
Congenital absence of epiglottis Finding site Epiglottis structure true Inferred relationship Existential restriction modifier 1
Congenital absence of epiglottis Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital absence of epiglottis Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Congenital absence of epiglottis Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 1
Congenital absence of epiglottis Associated morphology Absence 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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