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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
458765013 Retinal dystrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character 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
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
5213821000241116 dystrophie rétinienne fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
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 (disorder) Is a Retinal disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Retinal dystrophy (disorder) Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept)
Retinal dystrophy (disorder) Is a Degenerative disorder of eye (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Retinal dystrophy (disorder) Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Retinal dystrophy (disorder) Finding site Retinal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Retinal dystrophy (disorder) Is a Degeneration of retina (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary retinal dystrophy (disorder) Is a True Retinal dystrophy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Optic atrophy associated with retinal dystrophy Associated with True Retinal dystrophy (disorder) Inferred relationship Existential restriction modifier (core metadata concept) 2
Sensory retinal dystrophy Is a True Retinal dystrophy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Retinal pigment epithelial dystrophy (disorder) Is a True Retinal dystrophy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Alstrom syndrome Has definitional manifestation False Retinal dystrophy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Retinal dystrophy due to systemic disorder (disorder) Is a True Retinal dystrophy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Alstrom syndrome Is a False Retinal dystrophy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Renal dysplasia and retinal aplasia Is a True Retinal dystrophy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Ectopia lentis, chorioretinal dystrophy, myopia syndrome (disorder) Is a True Retinal dystrophy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Retinal dystrophy due to GM2 gangliosidosis Is a True Retinal dystrophy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Adult vitelliform macular dystrophy Is a True Retinal dystrophy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Best vitelliform macular dystrophy (disorder) Is a True Retinal dystrophy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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