88520007: Creutzfeldt-Jakob agent (organism)

SNOMED CT Concept\Organism (organism)\Prion\Spongiform encephalopathy agent\Human spongiform encephalopathy agent\Creutzfeldt-Jakob agent

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

146772012 Creutzfeldt-Jakob agent en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

146773019 Jakob-Creutzfeldt agent en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

831221012 Creutzfeldt-Jakob agent (organism) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

1235354019 Creutzfeldt-Jakob disease agent en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

4512181000005112 agens forårsagende Creutzfeldt-Jakobs sygdom da Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Danish module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Creutzfeldt-Jakob agent	Is a	Human spongiform encephalopathy agent	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Bovine spongiform encephalopathy agent	Is a	False	Creutzfeldt-Jakob agent	Inferred relationship	Some
Creutzfeldt-Jakob disease	Causative agent	False	Creutzfeldt-Jakob agent	Inferred relationship	Some
Variant Creutzfeldt-Jakob disease (disorder)	Causative agent	False	Creutzfeldt-Jakob agent	Inferred relationship	Some
Sporadic Creutzfeldt-Jakob disease (disorder)	Causative agent	False	Creutzfeldt-Jakob agent	Inferred relationship	Some	2
Creutzfeldt-Jakob disease	Causative agent	True	Creutzfeldt-Jakob agent	Inferred relationship	Some	1
Iatrogenic Jakob-Creutzfeldt disease (disorder)	Causative agent	True	Creutzfeldt-Jakob agent	Inferred relationship	Some	1
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.	Causative agent	True	Creutzfeldt-Jakob agent	Inferred relationship	Some	1
Classical sporadic Creutzfeldt-Jakob disease	Causative agent	True	Creutzfeldt-Jakob agent	Inferred relationship	Some	1
Creutzfeldt-Jakob Disease caused by human growth hormone	Causative agent	False	Creutzfeldt-Jakob agent	Inferred relationship	Some	1
Creutzfeldt Jakob disease following graft of dura (disorder)	Causative agent	True	Creutzfeldt-Jakob agent	Inferred relationship	Some	1
Sporadic fatal insomnia	Causative agent	True	Creutzfeldt-Jakob agent	Inferred relationship	Some	1
Creutzfeldt-Jakob Disease caused by human growth hormone	Causative agent	True	Creutzfeldt-Jakob agent	Inferred relationship	Some	2
Sporadic Creutzfeldt-Jakob disease (disorder)	Causative agent	True	Creutzfeldt-Jakob agent	Inferred relationship	Some	1

This concept is not in any reference sets