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253213006: Congenital ankyloblepharon (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
377110018 Congenital ankyloblepharon en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
377111019 Ankyloblepharon totale en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
377112014 Fused eyelids en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
643945013 Congenital ankyloblepharon (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3015206015 Blepharosynechia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5069751000241114 ankyloblépharon congénital fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
621071000274119 Totales Ankyloblepharon de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
621081000274117 Kongenitales Ankyloblepharon de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

4 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital ankyloblepharon Is a Congenital structural abnormality of eyelid true Inferred relationship Some
Congenital ankyloblepharon Associated morphology anomalie congénitale false Inferred relationship Some 1
Congenital ankyloblepharon Occurrence Congenital false Inferred relationship Some
Congenital ankyloblepharon Finding site Eyelid structure false Inferred relationship Some 2
Congenital ankyloblepharon Finding site Structure of orbit proper false Inferred relationship Some 2
Congenital ankyloblepharon Associated morphology anomalie congénitale false Inferred relationship Some 2
Congenital ankyloblepharon Associated morphology anomalie congénitale false Inferred relationship Some 2
Congenital ankyloblepharon Associated morphology anomalie congénitale false Inferred relationship Some 2
Congenital ankyloblepharon Associated morphology anomalie congénitale false Inferred relationship Some 2
Congenital ankyloblepharon Is a Ankyloblepharon true Inferred relationship Some
Congenital ankyloblepharon Finding site Structure of free margin of eyelid false Inferred relationship Some 1
Congenital ankyloblepharon Associated morphology Adhesion false Inferred relationship Some 1
Congenital ankyloblepharon Finding site Structure of free margin of eyelid false Inferred relationship Some 2
Congenital ankyloblepharon Associated morphology Adhesion true Inferred relationship Some 1
Congenital ankyloblepharon Associated morphology anomalie congénitale false Inferred relationship Some 2
Congenital ankyloblepharon Finding site Eyelid structure false Inferred relationship Some 2
Congenital ankyloblepharon Occurrence Congenital false Inferred relationship Some 2
Congenital ankyloblepharon Associated morphology anomalie du développement false Inferred relationship Some 3
Congenital ankyloblepharon Finding site Eyelid structure false Inferred relationship Some 3
Congenital ankyloblepharon Occurrence Congenital true Inferred relationship Some 1
Congenital ankyloblepharon Finding site Structure of free margin of eyelid true Inferred relationship Some 1
Congenital ankyloblepharon Associated morphology Congenital adhesion false Inferred relationship Some 2
Congenital ankyloblepharon Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Ankyloblepharon filiforme adnatum (disorder) Is a True Congenital ankyloblepharon Inferred relationship Some
Microphthalmia-ankyloblepharon-intellectual disability syndrome is characterized by microphthalmia, ankyloblepharon and intellectual deficit. It has been described in seven male patients from two generations of a Northern Ireland family. The causative gene is localized to the Xq27-q28 region. The syndrome is transmitted as an X-linked recessive trait. Is a True Congenital ankyloblepharon Inferred relationship Some

This concept is not in any reference sets

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