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312957005: Variant central serous chorioretinopathy (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
456774015 Variant central serous chorioretinopathy en Synonym Active Case insensitive SNOMED CT core
709686013 Variant central serous chorioretinopathy (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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