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708541009: Complete ablepharon (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2015. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3034825014 Congenital absence of eyelid en Synonym Active Entire term case insensitive SNOMED CT core module
3034841010 Complete ablepharon en Synonym Active Entire term case insensitive SNOMED CT core module
3034852016 Agenesis of eyelid en Synonym Active Entire term case insensitive SNOMED CT core module
3034859013 Complete ablepharon (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
Complete ablepharon Is a Ablepharon true Inferred relationship Existential restriction modifier
Complete ablepharon Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 1
Complete ablepharon Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Complete ablepharon Finding site Entire eyelid true Inferred relationship Existential restriction modifier 1
Complete ablepharon Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Complete ablepharon Associated morphology Agenesis 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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