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708541009: Complete ablepharon (disorder)


Status: current, Defined. Date: 31-Jan 2015. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3034825014 Congenital absence of eyelid en Synonym Active Case insensitive SNOMED CT core
3034841010 Complete ablepharon en Synonym Active Case insensitive SNOMED CT core
3034852016 Agenesis of eyelid en Synonym Active Case insensitive SNOMED CT core
3034859013 Complete ablepharon (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Complete ablepharon Pathological process Pathological developmental process true Inferred relationship Some 1
Complete ablepharon Associated morphology Agenesis true Inferred relationship Some 1
Complete ablepharon Is a Ablepharon true Inferred relationship Some
Complete ablepharon Associated morphology Congenital absence false Inferred relationship Some 1
Complete ablepharon Occurrence Congenital true Inferred relationship Some 1
Complete ablepharon Finding site Entire eyelid 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

Problem/Diagnosis reference set

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