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304603007: Variant Creutzfeldt-Jakob disease (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
446957016 nvCJD - New variant of Creutzfeldt-Jakob disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2528998014 Variant Creutzfeldt-Jakob disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2532511011 Variant Creutzfeldt-Jakob disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2536161012 vCJD - variant Creutzfeldt-Jakob disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3028936018 Creutzfeldt-Jakob variant disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
195791000077111 variante de la maladie de Creutzfeldt-Jakob fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
583001000274114 vCJK - Variante Creutzfeld-Jakob-Krankheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
583011000274111 Variante Creutzfeld-Jakob-Krankheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
2400061000195114 nvCJD - Variante der Creutzfeldt-Jakob-Krankheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
2400071000195115 Variante der Creutzfeldt-Jakob-Krankheit 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 Creutzfeldt-Jakob disease (disorder) Is a Creutzfeldt-Jakob disease false Inferred relationship Some
Variant Creutzfeldt-Jakob disease (disorder) Finding site Structure of central nervous system (body structure) false Inferred relationship Some 1
Variant Creutzfeldt-Jakob disease (disorder) Causative agent (attribute) Bovine spongiform encephalopathy agent false Inferred relationship Some
Variant Creutzfeldt-Jakob disease (disorder) Occurrence Congenital false Inferred relationship Some
Variant Creutzfeldt-Jakob disease (disorder) Pathological process Infectious disease false Inferred relationship Some
Variant Creutzfeldt-Jakob disease (disorder) Associated morphology Spongy degeneration false Inferred relationship Some 1
Variant Creutzfeldt-Jakob disease (disorder) Finding site Structure of telencephalon false Inferred relationship Some
Variant Creutzfeldt-Jakob disease (disorder) Finding site The cerebrum is the regional structure of the brain, which is the adult equivalent of the forebrain or prosencephalon. It is constituted by the structural derivatives of the telencephalon and diencephalon including the cerebral hemispheres, epithalamus, thalamus, hypothalamus, lateral ventricles and third ventricle. This definition is harmonious with the Federation of Association of Anatomist Second Edition (2019) Part V Terminologia Anatomica. false Inferred relationship Some 1
Variant Creutzfeldt-Jakob disease (disorder) Causative agent (attribute) Creutzfeldt-Jakob agent false Inferred relationship Some
Variant Creutzfeldt-Jakob disease (disorder) Has definitional manifestation Dementia false Inferred relationship Some
Variant Creutzfeldt-Jakob disease (disorder) Finding site The cerebrum is the regional structure of the brain, which is the adult equivalent of the forebrain or prosencephalon. It is constituted by the structural derivatives of the telencephalon and diencephalon including the cerebral hemispheres, epithalamus, thalamus, hypothalamus, lateral ventricles and third ventricle. This definition is harmonious with the Federation of Association of Anatomist Second Edition (2019) Part V Terminologia Anatomica. false Inferred relationship Some 1
Variant Creutzfeldt-Jakob disease (disorder) Associated morphology Spongy degeneration true Inferred relationship Some 1
Variant Creutzfeldt-Jakob disease (disorder) Pathological process (attribute) Infectious process (qualifier value) false Inferred relationship Some
Variant Creutzfeldt-Jakob disease (disorder) Causative agent (attribute) Prion false Inferred relationship Some 2
Variant Creutzfeldt-Jakob disease (disorder) Associated morphology Spongy degeneration false Inferred relationship Some 2
Variant Creutzfeldt-Jakob disease (disorder) Finding site Brain tissue structure false Inferred relationship Some 2
Variant Creutzfeldt-Jakob disease (disorder) Pathological process (attribute) Infectious process (qualifier value) false Inferred relationship Some 2
Variant Creutzfeldt-Jakob disease (disorder) Is a Prion disease true Inferred relationship Some
Variant Creutzfeldt-Jakob disease (disorder) Associated morphology Spongy degeneration false Inferred relationship Some 3
Variant Creutzfeldt-Jakob disease (disorder) Causative agent (attribute) Bovine spongiform encephalopathy agent false Inferred relationship Some 3
Variant Creutzfeldt-Jakob disease (disorder) Finding site Brain tissue structure false Inferred relationship Some 3
Variant Creutzfeldt-Jakob disease (disorder) Pathological process (attribute) Infectious process (qualifier value) false Inferred relationship Some 3
Variant Creutzfeldt-Jakob disease (disorder) Finding site Brain structure true Inferred relationship Some 1
Variant Creutzfeldt-Jakob disease (disorder) Pathological process (attribute) Infectious process (qualifier value) true Inferred relationship Some 1
Variant Creutzfeldt-Jakob disease (disorder) Causative agent (attribute) Bovine spongiform encephalopathy agent true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
At increased risk of variant Creutzfeldt-Jakob disease (finding) This attribute specifies the realization of a function True Variant Creutzfeldt-Jakob disease (disorder) Inferred relationship Some 2
Dementia due to variant Creutzfeldt-Jakob disease (disorder) Due to True Variant Creutzfeldt-Jakob disease (disorder) Inferred relationship Some 3

This concept is not in any reference sets

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