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314407005: Retinal 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
458765013 Retinal dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
711209016 Retinal dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5213821000241116 dystrophie rétinienne fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
554821000274116 Netzhautdystrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
605941000274118 Retinadystrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


118 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Retinal dystrophy Is a Retinal disorder false Inferred relationship Some
Retinal dystrophy Finding site Retinal structure false Inferred relationship Some
Retinal dystrophy Is a Degenerative disorder of eye false Inferred relationship Some
Retinal dystrophy Associated morphology Dystrophy true Inferred relationship Some 1
Retinal dystrophy Finding site Retinal structure true Inferred relationship Some 1
Retinal dystrophy Is a Degeneration of retina true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary retinal dystrophy Is a True Retinal dystrophy Inferred relationship Some
Optic atrophy associated with retinal dystrophy Associated with True Retinal dystrophy Inferred relationship Some 2
Sensory retinal dystrophy Is a True Retinal dystrophy Inferred relationship Some
Retinal pigment epithelial dystrophy Is a True Retinal dystrophy Inferred relationship Some
Alstrom syndrome Has definitional manifestation False Retinal dystrophy Inferred relationship Some
Retinal dystrophy due to systemic disorder (disorder) Is a True Retinal dystrophy Inferred relationship Some
Alstrom syndrome Is a False Retinal dystrophy Inferred relationship Some
Renal dysplasia and retinal aplasia Is a True Retinal dystrophy Inferred relationship Some
A rare, genetic, ophthalmic disorder characterized by the association of lens (ectopia and cataracts) and retinal (generalized tapetoretinal dystrophy and retinal detachment) anomalies, and variable myopia. Microcephaly and intellectual disability have been reported in some patients. Is a True Retinal dystrophy Inferred relationship Some
Retinal dystrophy due to GM2 gangliosidosis Is a True Retinal dystrophy Inferred relationship Some
A rare, genetic, macular dystrophy characterized by blurred vision, metamorphopsia and mild visual impairment secondary to a slightly elevated, yellow, egg yolk-like lesion located in the foveal or parafoveal region. Is a True Retinal dystrophy Inferred relationship Some
Best vitelliform macular dystrophy (BVMD) is a genetic macular dystrophy characterized by loss of central visual acuity, metamorphopsia and a decrease in the Arden ratio secondary to an egg yolk-like lesion located in the foveal or parafoveal region. Is a True Retinal dystrophy Inferred relationship Some

This concept is not in any reference sets

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