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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
7275661000241115 taches rétiniennes fr Synonym (core metadata concept) Active Entire term case insensitive (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 Is a Retinal deposits true Inferred relationship Some
Retinal flecking Associated morphology Deposition false Inferred relationship Some 1
Retinal flecking Finding site Retinal structure false Inferred relationship Some 1
Retinal flecking Associated morphology Deposition true Inferred relationship Some 1
Retinal flecking Finding site Retinal structure true Inferred relationship Some 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 Inferred relationship Some
Kandori fleck retina is a rare, genetic retinal dystrophy disorder characterized by irregular, sharply defined, yellowish-white lesions of variable size that are distributed mainly in the nasal equatorial region of the retina, with a tendency to confluence, that are not associated with any vascular or optic nerve abnormalities. They frequently manifest as mild and stationary night blindness. Is a True Retinal flecking Inferred relationship Some

This concept is not in any reference sets

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