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247138002: Retinal flecking (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
369076012 Retinal flecking en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
637272010 Retinal flecking (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
369076012 Retinal flecking en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
369076012 Retinal flecking en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
637272010 Retinal flecking (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
637272010 Retinal flecking (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
522161000274110 Flecken auf Netzhaut de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
562481000274117 Flecken auf Retina de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
522161000274110 Flecken auf Netzhaut de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
562481000274117 Flecken auf Retina 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
Retinal flecking (disorder) Is a Retinal deposits true Inferred relationship Existential restriction modifier (core metadata concept)
Retinal flecking (disorder) Associated morphology Deposition false Inferred relationship Existential restriction modifier (core metadata concept) 1
Retinal flecking (disorder) Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Retinal flecking (disorder) Associated morphology Deposition true Inferred relationship Existential restriction modifier (core metadata concept) 1
Retinal flecking (disorder) Finding site Retinal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Familial benign flecked retina is a rare retinal dystrophy characterized by diffuse bilateral white-yellow fleck-like lesions extending to the far periphery of the retina but sparing the foveal region, with asymptomatic clinical phenotype and absence of electrophysiologic deficits. Is a True Retinal flecking (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Kandori fleck retina syndrome (disorder) Is a True Retinal flecking (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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