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304603007: Variant Creutzfeldt-Jakob disease (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
2528998014 Variant Creutzfeldt-Jakob disease (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
2532511011 Variant Creutzfeldt-Jakob disease en Synonym Active Initial character case insensitive SNOMED CT core
2536161012 vCJD - variant Creutzfeldt-Jakob disease en Synonym Active Case sensitive SNOMED CT core
3028936018 Creutzfeldt-Jakob variant disease en Synonym Active Case sensitive SNOMED CT core
446957016 nvCJD - New variant of Creutzfeldt-Jakob disease en Synonym Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Variant Creutzfeldt-Jakob disease Is a Jakob-Creutzfeldt disease false Inferred relationship Some
Variant Creutzfeldt-Jakob disease Finding site Structure of cerebrum false Inferred relationship Some 1
Variant Creutzfeldt-Jakob disease Causative agent Creutzfeldt-Jakob agent false Inferred relationship Some
Variant Creutzfeldt-Jakob disease Has definitional manifestation Dementia false Inferred relationship Some
Variant Creutzfeldt-Jakob disease Finding site Structure of cerebrum false Inferred relationship Some 1
Variant Creutzfeldt-Jakob disease Associated morphology Spongy degeneration false Inferred relationship Some 1
Variant Creutzfeldt-Jakob disease Pathological process Infectious process false Inferred relationship Some
Variant Creutzfeldt-Jakob disease Finding site Structure of central nervous system false Inferred relationship Some 1
Variant Creutzfeldt-Jakob disease Causative agent Prion false Inferred relationship Some 2
Variant Creutzfeldt-Jakob disease Associated morphology Spongy degeneration false Inferred relationship Some 2
Variant Creutzfeldt-Jakob disease Finding site Brain tissue structure false Inferred relationship Some 2
Variant Creutzfeldt-Jakob disease Pathological process Infectious process false Inferred relationship Some 2
Variant Creutzfeldt-Jakob disease Is a Prion disease true Inferred relationship Some
Variant Creutzfeldt-Jakob disease Associated morphology Spongy degeneration true Inferred relationship Some 3
Variant Creutzfeldt-Jakob disease Causative agent Bovine spongiform encephalopathy agent true Inferred relationship Some 3
Variant Creutzfeldt-Jakob disease Finding site Brain tissue structure true Inferred relationship Some 3
Variant Creutzfeldt-Jakob disease Pathological process Infectious process true Inferred relationship Some 3
Variant Creutzfeldt-Jakob disease Causative agent Bovine spongiform encephalopathy agent false Inferred relationship Some
Variant Creutzfeldt-Jakob disease Occurrence Congenital false Inferred relationship Some
Variant Creutzfeldt-Jakob disease Pathological process Infection false Inferred relationship Some
Variant Creutzfeldt-Jakob disease Associated morphology Spongy degeneration false Inferred relationship Some 1
Variant Creutzfeldt-Jakob disease Finding site Structure of telencephalon false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Dementia due to variant Creutzfeldt-Jakob disease Due to True Variant Creutzfeldt-Jakob disease Inferred relationship Some 3

Reference Sets

Disease caused by microorganism or bacterial toxin reference set

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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