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723408004: Multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5403045013 A rare, patterned dystrophy of the retinal pigment epithelium characterized by multiple yellowish irregular flecks scattered or interconnected around the macula, simulating what is observed in Stargardt disease, and usually asymptomatic until adulthood when patients present with a slowly progressive loss of vision that often only becomes apparent in old age. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403046014 A rare, patterned dystrophy of the retinal pigment epithelium characterised by multiple yellowish irregular flecks scattered or interconnected around the macula, simulating what is observed in Stargardt disease, and usually asymptomatic until adulthood when patients present with a slowly progressive loss of vision that often only becomes apparent in old age. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3424464010 Multifocal pattern dystrophy simulating Stargardt disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3424466012 Multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3424467015 Multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3424468013 Multifocal pattern dystrophy simulating fundus flavimaculatus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
7609751000241118 dystrophie multifocale de l'épithélium pigmentaire de la rétine simulant un fundus flavimaculatus fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
173841000274116 Multifokale Musterdystrophie mit vorgetäuschter Fundus flavimaculatus de Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
A rare, patterned dystrophy of the retinal pigment epithelium characterized by multiple yellowish irregular flecks scattered or interconnected around the macula, simulating what is observed in Stargardt disease, and usually asymptomatic until adulthood when patients present with a slowly progressive loss of vision that often only becomes apparent in old age. Is a Autosomal dominant hereditary disorder (disorder) true Inferred relationship Some
A rare, patterned dystrophy of the retinal pigment epithelium characterized by multiple yellowish irregular flecks scattered or interconnected around the macula, simulating what is observed in Stargardt disease, and usually asymptomatic until adulthood when patients present with a slowly progressive loss of vision that often only becomes apparent in old age. Is a Hereditary disorder of the visual system false Inferred relationship Some
A rare, patterned dystrophy of the retinal pigment epithelium characterized by multiple yellowish irregular flecks scattered or interconnected around the macula, simulating what is observed in Stargardt disease, and usually asymptomatic until adulthood when patients present with a slowly progressive loss of vision that often only becomes apparent in old age. Is a Retinal pigment epithelial dystrophy false Inferred relationship Some
A rare, patterned dystrophy of the retinal pigment epithelium characterized by multiple yellowish irregular flecks scattered or interconnected around the macula, simulating what is observed in Stargardt disease, and usually asymptomatic until adulthood when patients present with a slowly progressive loss of vision that often only becomes apparent in old age. Associated morphology Dystrophy true Inferred relationship Some 1
A rare, patterned dystrophy of the retinal pigment epithelium characterized by multiple yellowish irregular flecks scattered or interconnected around the macula, simulating what is observed in Stargardt disease, and usually asymptomatic until adulthood when patients present with a slowly progressive loss of vision that often only becomes apparent in old age. Finding site Structure of retinal pigment epithelium true Inferred relationship Some 1
A rare, patterned dystrophy of the retinal pigment epithelium characterized by multiple yellowish irregular flecks scattered or interconnected around the macula, simulating what is observed in Stargardt disease, and usually asymptomatic until adulthood when patients present with a slowly progressive loss of vision that often only becomes apparent in old age. Is a Hereditary retinal dystrophy primarily involving retinal pigment epithelium true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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