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342581000119102: Retinal pigment epithelial dystrophy (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2990119012 Retinal pigment epithelial dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2740571000119117 Retinal pigment epithelial dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
7817911000241115 dystrophie de l'EPR (épithélium pigmentaire rétinien) fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
7817921000241110 dystrophie de l'épithélium pigmentaire rétinien fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
514371000274115 Pigmentepitheldystrophie der Retinae de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
586051000274118 Retinale Pigmentepitheldystrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


9 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Retinal pigment epithelial dystrophy Is a Retinal pigment epithelial abnormality true Inferred relationship Some
Retinal pigment epithelial dystrophy Associated morphology Dystrophy true Inferred relationship Some 1
Retinal pigment epithelial dystrophy Finding site Structure of retinal pigment epithelium true Inferred relationship Some 1
Retinal pigment epithelial dystrophy Is a Retinal dystrophy true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
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 False Retinal pigment epithelial dystrophy Inferred relationship Some
A rare, patterned dystrophy of the retinal pigment epithelium, of progressive course, characterized by the presence of a bilateral hyperpigmented reticular pattern resembling a fishnet with knots, resulting in a slowly progressive loss of vision that often only becomes apparent in old age. This disorder is sometimes associated with scleral staphyloma, choroidal neovascularization, convergent strabismus, spherophakia with myopia and luxated lenses, and partial atrophy of the iris. Is a False Retinal pigment epithelial dystrophy Inferred relationship Some
Pattern dystrophy of macula Is a False Retinal pigment epithelial dystrophy Inferred relationship Some
Fundus pulverulentus is a rare form of patterned dystrophy of the retinal pigment epithelium characterized by a granular appearance in the macula, with coarse and punctiform mottling of the retinal pigment epithelium within the macular region. Association with choroidal neovascularization has been reported. Is a True Retinal pigment epithelial dystrophy Inferred relationship Some
Saldino-Mainzer dysplasia Is a True Retinal pigment epithelial dystrophy Inferred relationship Some
Hereditary retinal dystrophy primarily involving retinal pigment epithelium Is a True Retinal pigment epithelial dystrophy Inferred relationship Some

This concept is not in any reference sets

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