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770434009: Familial benign flecked retina (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3700846017 Familial benign flecked retina en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3700847014 Familial benign flecked retina (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5404792013 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404793015 Familial benign flecked retina is a rare retinal dystrophy characterised 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3700846017 Familial benign flecked retina en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3700847014 Familial benign flecked retina (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3700848016 A rare retinal dystrophy with characteristics of 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404792013 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404793015 Familial benign flecked retina is a rare retinal dystrophy characterised 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
543991000274113 Benigne familiäre gefleckte Netzhaut de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
574421000274116 Benigne familiäre gefleckte Retina de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
901281000172113 rétine tachetée familiale bénigne fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
901281000172113 rétine tachetée familiale bénigne fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
543991000274113 Benigne familiäre gefleckte Netzhaut de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
574421000274116 Benigne familiäre gefleckte Retina de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3414141001000117 Gefleckte Retina, benigne familiäre 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
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 Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
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. Finding site Retinal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
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 Hereditary retinal dystrophy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
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 Retinal flecking (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
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. Finding site Retinal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
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. Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
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. Associated morphology Deposition true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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