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792004: Jakob-Creutzfeldt disease (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2386018 Jakob-Creutzfeldt disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2387010 Creutzfeldt-Jakob disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2388017 Subacute spongiform encephalopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
820225015 Jakob-Creutzfeldt disease (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
1234325017 CJD - Creutzfeldt-Jakob disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1234326016 JCD - Jakob-Creutzfeldt disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2164150017 Transmissible virus dementia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1850761000195114 malattia di Jakob-Creutzfeldt it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
195271000077119 maladie de Creutzfeldt-Jakob fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
903691000195119 Jakob-Creutzfeld Krankheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
2347361000195113 Creutzfeldt-Jakob-Krankheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
2347371000195119 Subakute spongiforme Enzephalopathie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
2347381000195117 CJK - Creutzfeldt-Jakob-Krankheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


7 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Creutzfeldt-Jakob disease Is a syndrome cérébral non spécifique false Inferred relationship Some
Creutzfeldt-Jakob disease Is a Congenital anomaly of head false Inferred relationship Some
Creutzfeldt-Jakob disease Is a Prion disease true Inferred relationship Some
Creutzfeldt-Jakob disease Is a Spongy degeneration of central nervous system false Inferred relationship Some
Creutzfeldt-Jakob disease Finding site Structure of central nervous system (body structure) false Inferred relationship Some 1
Creutzfeldt-Jakob disease Causative agent (attribute) Creutzfeldt-Jakob agent false Inferred relationship Some
Creutzfeldt-Jakob disease Pathological process Infectious disease false Inferred relationship Some
Creutzfeldt-Jakob disease Finding site Structure of telencephalon false Inferred relationship Some
Creutzfeldt-Jakob disease Occurrence Congenital false Inferred relationship Some
Creutzfeldt-Jakob disease Associated morphology Spongy degeneration false Inferred relationship Some 1
Creutzfeldt-Jakob disease Finding site Brain tissue structure false Inferred relationship Some 1
Creutzfeldt-Jakob disease Has definitional manifestation Dementia false Inferred relationship Some
Creutzfeldt-Jakob disease 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 2
Creutzfeldt-Jakob disease Associated morphology dégénérescence false Inferred relationship Some 2
Creutzfeldt-Jakob disease Finding site Brain tissue structure false Inferred relationship Some 1
Creutzfeldt-Jakob disease Associated morphology Spongy degeneration true Inferred relationship Some 1
Creutzfeldt-Jakob disease Associated morphology dégénérescence false Inferred relationship Some 2
Creutzfeldt-Jakob disease 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 2
Creutzfeldt-Jakob disease Pathological process (attribute) Infectious process (qualifier value) false Inferred relationship Some
Creutzfeldt-Jakob disease Causative agent (attribute) Prion false Inferred relationship Some 3
Creutzfeldt-Jakob disease Associated morphology Spongy degeneration false Inferred relationship Some 3
Creutzfeldt-Jakob disease Finding site Brain tissue structure false Inferred relationship Some 3
Creutzfeldt-Jakob disease Pathological process (attribute) Infectious process (qualifier value) false Inferred relationship Some 3
Creutzfeldt-Jakob disease Causative agent (attribute) Creutzfeldt-Jakob agent true Inferred relationship Some 1
Creutzfeldt-Jakob disease Pathological process (attribute) Infectious process (qualifier value) true Inferred relationship Some 1
Creutzfeldt-Jakob disease Finding site Brain structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Variant Creutzfeldt-Jakob disease (disorder) Is a False Creutzfeldt-Jakob disease Inferred relationship Some
Bovine spongiform encephalopathy Is a False Creutzfeldt-Jakob disease Inferred relationship Some
Cerebral degeneration due to Creutzfeldt-Jakob disease Due to True Creutzfeldt-Jakob disease Inferred relationship Some 2
Dementia due to Creutzfeldt Jakob disease (disorder) Due to True Creutzfeldt-Jakob disease Inferred relationship Some 2
Sporadic Creutzfeldt-Jakob disease (disorder) Is a True Creutzfeldt-Jakob disease Inferred relationship Some
Iatrogenic Jakob-Creutzfeldt disease (disorder) Is a True Creutzfeldt-Jakob disease Inferred relationship Some
Inherited or familial Creutzfeldt-Jakob disease (fCJD) is a very rare form of genetic prion disease characterized by typical CJD features (rapidly progressive dementia, personality/behavioral changes, psychiatric disorders, myoclonus, and ataxia) with a genetic cause and sometimes a family history of dementia. Is a True Creutzfeldt-Jakob disease Inferred relationship Some
Creutzfeldt Jakob disease following graft of dura (disorder) Is a False Creutzfeldt-Jakob disease Inferred relationship Some

This concept is not in any reference sets

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