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708541009: Complete ablepharon (disorder)


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

Descriptions:

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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Complete ablepharon Is a Ablepharon true Inferred relationship Some
Complete ablepharon Associated morphology Congenital absence (morphologic abnormality) 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
Complete ablepharon Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Complete ablepharon Associated morphology Agenesis (morphologic abnormality) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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