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13282008: Congenital corneal opacity interfering with vision (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
22729014 Congenital corneal opacity interfering with vision en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
737420015 Congenital corneal opacity interfering with vision (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
22729014 Congenital corneal opacity interfering with vision en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
22729014 Congenital corneal opacity interfering with vision en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
737420015 Congenital corneal opacity interfering with vision (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
737420015 Congenital corneal opacity interfering with vision (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
638421000274118 Kongenitale Hornhauttrübung mit Beeinträchtigung des Sehvermögens de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
638431000274116 Kongenitale Trübung der Kornea mit Beeinträchtigung des Sehvermögens de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4433291000241119 opacité de la cornée congénitale gênant la vision fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4433291000241119 opacité de la cornée congénitale gênant la vision fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
638421000274118 Kongenitale Hornhauttrübung mit Beeinträchtigung des Sehvermögens de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
638431000274116 Kongenitale Trübung der Kornea mit Beeinträchtigung des Sehvermögens de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital corneal opacity interfering with vision (disorder) Is a Congenital structural abnormality of cornea true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital corneal opacity interfering with vision (disorder) Is a Corneal opacity true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital corneal opacity interfering with vision (disorder) Finding site Nervous system structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital corneal opacity interfering with vision (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital corneal opacity interfering with vision (disorder) Finding site Corneal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital corneal opacity interfering with vision (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital corneal opacity interfering with vision (disorder) Finding site Orbital region structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital corneal opacity interfering with vision (disorder) Associated morphology Opacity true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital corneal opacity interfering with vision (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital corneal opacity interfering with vision (disorder) Finding site Corneal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital corneal opacity interfering with vision (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital corneal opacity interfering with vision (disorder) Finding site Corneal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital corneal opacity interfering with vision (disorder) Finding site Corneal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital corneal opacity interfering with vision (disorder) Finding site Corneal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital corneal opacity interfering with vision (disorder) Finding site Corneal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital corneal opacity interfering with vision (disorder) Finding site Corneal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital corneal opacity interfering with vision (disorder) Finding site Corneal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital corneal opacity interfering with vision (disorder) Finding site Corneal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital corneal opacity interfering with vision (disorder) Finding site Corneal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital corneal opacity interfering with vision (disorder) Finding site Corneal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital corneal opacity interfering with vision (disorder) Finding site Corneal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital corneal opacity interfering with vision (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital corneal opacity interfering with vision (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital corneal opacity interfering with vision (disorder) Finding site Corneal structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital corneal opacity interfering with vision (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital corneal opacity interfering with vision (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital corneal opacity interfering with vision (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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