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312957005: variant van centrale sereuze chorioretinopathie (aandoening)


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
9959391000146110 variant van centrale sereuze chorioretinopathie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
9959401000146113 variant van centrale sereuze chorioretinopathie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Variant central serous chorioretinopathy (disorder) Is a Central serous chorioretinopathy true Inferred relationship Some
Variant central serous chorioretinopathy (disorder) Is a Central serous retinopathy false Inferred relationship Some
Variant central serous chorioretinopathy (disorder) Finding site Central retina area false Inferred relationship Some
Variant central serous chorioretinopathy (disorder) Associated morphology Separation (morphologic abnormality) false Inferred relationship Some 1
Variant central serous chorioretinopathy (disorder) Finding site Structure of posterior pole of eye false Inferred relationship Some
Variant central serous chorioretinopathy (disorder) Finding site Retinal structure false Inferred relationship Some 1
Variant central serous chorioretinopathy (disorder) Finding site Retinal structure false Inferred relationship Some 1
Variant central serous chorioretinopathy (disorder) Associated morphology Separation (morphologic abnormality) false Inferred relationship Some 1
Variant central serous chorioretinopathy (disorder) Associated morphology Separation (morphologic abnormality) true Inferred relationship Some 2
Variant central serous chorioretinopathy (disorder) Finding site Neuroepithelial layer true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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