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13401001: Ablepharon (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2005. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
22906014 Ablepharon en Synonym Active Entire term case insensitive SNOMED CT core module
22909019 Ablepharia en Synonym Active Entire term case insensitive SNOMED CT core module
22910012 Open eye en Synonym Active Entire term case insensitive SNOMED CT core module
738711014 Ablepharon (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1220954016 Ablepharon - absent eyelids en Synonym Active Entire term case insensitive SNOMED CT core module


10 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Ablepharon Is a Congenital anomaly of eyelid true Inferred relationship Existential restriction modifier
Ablepharon Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 1
Ablepharon Occurrence Congenital false Inferred relationship Existential restriction modifier
Ablepharon Finding site Eyelid structure false Inferred relationship Existential restriction modifier 1
Ablepharon Finding site Structure of orbit proper false Inferred relationship Existential restriction modifier 1
Ablepharon Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Ablepharon Is a Congenital malformation false Inferred relationship Existential restriction modifier
Ablepharon Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 1
Ablepharon Finding site Eyelid structure false Inferred relationship Existential restriction modifier 1
Ablepharon Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Ablepharon Finding site Eyelid structure false Inferred relationship Existential restriction modifier 2
Ablepharon Is a Congenital absence false Inferred relationship Existential restriction modifier
Ablepharon Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 2
Ablepharon Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Ablepharon Finding site Eyelid structure true Inferred relationship Existential restriction modifier 1
Ablepharon Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Ablepharon Associated morphology Aplasia false Inferred relationship Existential restriction modifier 1
Ablepharon Associated morphology Absence true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Partial ablepharon Is a True Ablepharon Inferred relationship Existential restriction modifier
Agenesis of eyelid Is a False Ablepharon Inferred relationship Existential restriction modifier
Agenesis of punctum lacrimale Is a False Ablepharon Inferred relationship Existential restriction modifier
Congenital absence of eyelash Is a False Ablepharon Inferred relationship Existential restriction modifier
Complete ablepharon Is a True Ablepharon Inferred relationship Existential restriction modifier
Ablepharon macrostomia syndrome Is a True Ablepharon Inferred relationship Existential restriction modifier
Pseudoprogeria syndrome Is a False Ablepharon Inferred relationship Existential restriction modifier
Ablepharon of bilateral eyelids Is a True Ablepharon Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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