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312957005: Variant central serous chorioretinopathy (disorder)


Status: current, Not 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
456774015 Variant central serous chorioretinopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
709686013 Variant central serous chorioretinopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
456774015 Variant central serous chorioretinopathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
456774015 Variant central serous chorioretinopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
709686013 Variant central serous chorioretinopathy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
709686013 Variant central serous chorioretinopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
605221000274119 Variante der zentralen serösen Chorioretinopathie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
605221000274119 Variante der zentralen serösen Chorioretinopathie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Variant central serous chorioretinopathy (disorder) Is a Central serous chorioretinopathy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Variant central serous chorioretinopathy (disorder) Is a Central serous retinopathy false Inferred relationship Existential restriction modifier (core metadata concept)
Variant central serous chorioretinopathy (disorder) Finding site Central retina area false Inferred relationship Existential restriction modifier (core metadata concept)
Variant central serous chorioretinopathy (disorder) Associated morphology Separation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Variant central serous chorioretinopathy (disorder) Finding site Structure of posterior pole of eye (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Variant central serous chorioretinopathy (disorder) Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Variant central serous chorioretinopathy (disorder) Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Variant central serous chorioretinopathy (disorder) Associated morphology Separation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Variant central serous chorioretinopathy (disorder) Associated morphology Separation true Inferred relationship Existential restriction modifier (core metadata concept) 2
Variant central serous chorioretinopathy (disorder) Finding site Structure of neuroepithelial layer of retina (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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