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95494009: Retinal dysplasia (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
158174018 Retinal dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
839659010 Retinal dysplasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
158174018 Retinal dysplasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
158174018 Retinal dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
839659010 Retinal dysplasia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
839659010 Retinal dysplasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
513321000274117 Netzhautdysplasie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
627131000274113 Retinadysplasie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4730811000241114 dysplasie rétinienne fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4730811000241114 dysplasie rétinienne fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
513321000274117 Netzhautdysplasie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
627131000274113 Retinadysplasie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


7 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Retinal dysplasia Is a Congenital anomaly of retina true Inferred relationship Existential restriction modifier (core metadata concept)
Retinal dysplasia Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Retinal dysplasia Finding site Nervous system structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Retinal dysplasia Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Retinal dysplasia Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Retinal dysplasia Associated morphology Dysplasia false Inferred relationship Existential restriction modifier (core metadata concept)
Retinal dysplasia Finding site Retinal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Retinal dysplasia Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Retinal dysplasia Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Retinal dysplasia Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Retinal dysplasia Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Retinal dysplasia Is a Lesion of eye (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Retinal dysplasia Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Retinal dysplasia Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Retinal dysplasia Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Retinal dysplasia Is a Lesion of retina true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Septo-optic dysplasia sequence Is a False Retinal dysplasia Inferred relationship Existential restriction modifier (core metadata concept)
Multifocal retinal dysplasia Is a True Retinal dysplasia Inferred relationship Existential restriction modifier (core metadata concept)
Geographic retinal dysplasia Is a True Retinal dysplasia Inferred relationship Existential restriction modifier (core metadata concept)
Diffuse retinal dysplasia Is a True Retinal dysplasia Inferred relationship Existential restriction modifier (core metadata concept)
Septo-optic dysplasia sequence Is a False Retinal dysplasia Inferred relationship Existential restriction modifier (core metadata concept)
Vitreoretinal dysplasia Is a True Retinal dysplasia Inferred relationship Existential restriction modifier (core metadata concept)
X-linked retinal dysplasia (disorder) Is a True Retinal dysplasia Inferred relationship Existential restriction modifier (core metadata concept)
Optic disc dysplasia (disorder) Is a True Retinal dysplasia Inferred relationship Existential restriction modifier (core metadata concept)
Congenital retinal dysplasia caused by teratogenic substance (disorder) Is a True Retinal dysplasia Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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