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429449002: Congenital hypoplasia of fovea centralis (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2008. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2690878011 Congenital hypoplasia of fovea centralis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2693410016 Congenital hypoplasia of fovea centralis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2694076018 Congenital hypoplasia of fovea en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2690878011 Congenital hypoplasia of fovea centralis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2690878011 Congenital hypoplasia of fovea centralis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2693410016 Congenital hypoplasia of fovea centralis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2693410016 Congenital hypoplasia of fovea centralis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2694076018 Congenital hypoplasia of fovea en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2694076018 Congenital hypoplasia of fovea en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
512231000274118 Kongenitale Hypoplasie der Sehgrube de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
598811000274114 Kongenitale Hypoplasie der Fovea de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5309301000241112 Hypoplasie congénitale des fovea centralis fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5309301000241112 Hypoplasie congénitale des fovea centralis fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
512231000274118 Kongenitale Hypoplasie der Sehgrube de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
598811000274114 Kongenitale Hypoplasie der Fovea de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital hypoplasia of fovea centralis (disorder) Is a Congenital anomaly of macula true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of fovea centralis (disorder) Is a Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of fovea centralis (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of fovea centralis (disorder) Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of fovea centralis (disorder) Finding site Structure of fovea centralis false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of fovea centralis (disorder) Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of fovea centralis (disorder) Finding site Structure of fovea centralis true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of fovea centralis (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of fovea centralis (disorder) Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of fovea centralis (disorder) Finding site Structure of fovea centralis false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of fovea centralis (disorder) Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of fovea centralis (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of fovea centralis (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Foveal hypoplasia with presenile cataract syndrome Is a True Congenital hypoplasia of fovea centralis (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Foveal hypoplasia, optic nerve decussation defect, anterior segment dysgenesis syndrome Is a True Congenital hypoplasia of fovea centralis (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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