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268160006: Congenital corneal opacity (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
400780010 Congenital corneal opacity en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
660866012 Congenital corneal opacity (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
400780010 Congenital corneal opacity en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
400780010 Congenital corneal opacity en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
660866012 Congenital corneal opacity (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
660866012 Congenital corneal opacity (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
394451000274115 Angeborene Hornhauttrübung de Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
534031000274110 Kongenitale Hornhauttrübung de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
622741000274116 Kongenitale Trübung der Kornea de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5107681000241114 opacité de la cornée congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5107681000241114 opacité de la cornée congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
394451000274115 Angeborene Hornhauttrübung de Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
534031000274110 Kongenitale Hornhauttrübung de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
622741000274116 Kongenitale Trübung der Kornea de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

13 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital corneal opacity Is a Corneal opacity true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital corneal opacity Is a Congenital structural abnormality of cornea true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital corneal opacity Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital corneal opacity Finding site Nervous system structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital corneal opacity Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital corneal opacity Associated morphology Opacity false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital corneal opacity Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital corneal opacity Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital corneal opacity Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital corneal opacity Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital corneal opacity Finding site Corneal structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital corneal opacity Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital corneal opacity Associated morphology Congenital opacity false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital corneal opacity Finding site Corneal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital corneal opacity Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital corneal opacity Associated morphology Opacity true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital corneal opacity with visual deficit (disorder) Is a True Congenital corneal opacity Inferred relationship Existential restriction modifier (core metadata concept)
Congenital corneal opacity without visual deficit Is a True Congenital corneal opacity Inferred relationship Existential restriction modifier (core metadata concept)
Congenital corneal opacities NOS Is a False Congenital corneal opacity Inferred relationship Existential restriction modifier (core metadata concept)
Congenital corneal keloid (disorder) Is a False Congenital corneal opacity Inferred relationship Existential restriction modifier (core metadata concept)
Congenital sclerocornea Is a True Congenital corneal opacity Inferred relationship Existential restriction modifier (core metadata concept)
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) Is a False Congenital corneal opacity Inferred relationship Existential restriction modifier (core metadata concept)
Congenital opacity of cornea of left eye Is a True Congenital corneal opacity Inferred relationship Existential restriction modifier (core metadata concept)
Congenital opacity of cornea of right eye Is a True Congenital corneal opacity Inferred relationship Existential restriction modifier (core metadata concept)
de Barsey syndrome Is a True Congenital corneal opacity Inferred relationship Existential restriction modifier (core metadata concept)
Congenital corneal leucoma Is a True Congenital corneal opacity Inferred relationship Existential restriction modifier (core metadata concept)
A rare genetic eye disease characterised by congenital cataract, microcornea, and corneal opacity, resulting in severe visual impairment or blindness. Depending on the genetic background, other developmental ocular defects may also be present. Is a True Congenital corneal opacity Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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