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20484008: Prion disease (disorder)


Status: current, 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 Reference Sets
34472014 Prion disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
749644017 Prion disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
4551687011 Transmissible spongiform encephalopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)

16 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Prion disease Is a Cerebral degeneration presenting primarily with dementia false Inferred relationship Some
Prion disease Is a Disorder due to infection false Inferred relationship Some
Prion disease Associated morphology Degeneration false Inferred relationship Some 1
Prion disease Finding site Structure of central nervous system (body structure) false Inferred relationship Some 1
Prion disease Pathological process Disorder due to infection false Inferred relationship Some
Prion disease Finding site Structure of telencephalon false Inferred relationship Some
Prion disease Causative agent Prion false Inferred relationship Some
Prion disease Is a Infectious disease of brain true Inferred relationship Some
Prion disease Is a Congenital anomaly of head false Inferred relationship Some
Prion disease Is a Spongy degeneration of central nervous system false Inferred relationship Some
Prion disease Is a Non-specific brain syndrome false Inferred relationship Some
Prion disease Occurrence Congenital false Inferred relationship Some
Prion disease Finding site Brain tissue structure false Inferred relationship Some 1
Prion disease Associated morphology Spongy degeneration false Inferred relationship Some 1
Prion disease Is a Congenital infectious disease false Inferred relationship Some
Prion disease Associated morphology Degeneration false Inferred relationship Some 2
Prion disease Finding site Cerebrum false Inferred relationship Some 2
Prion disease Has definitional manifestation Dementia false Inferred relationship Some
Prion disease Associated morphology Spongy degeneration false Inferred relationship Some 1
Prion disease Finding site Brain tissue structure false Inferred relationship Some 1
Prion disease Associated morphology Degeneration false Inferred relationship Some 2
Prion disease Finding site Cerebrum false Inferred relationship Some 2
Prion disease Pathological process (attribute) Infectious process (qualifier value) false Inferred relationship Some
Prion disease Is a Disorder due to infection false Inferred relationship Some
Prion disease Is a Infective disorder of head false Inferred relationship Some
Prion disease Causative agent Prion true Inferred relationship Some 3
Prion disease Associated morphology Spongy degeneration true Inferred relationship Some 3
Prion disease Finding site Brain tissue structure true Inferred relationship Some 3
Prion disease Pathological process (attribute) Infectious process (qualifier value) true Inferred relationship Some 3
Prion disease Is a Degenerative brain disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Spongiform encephalopathy Is a True Prion disease Inferred relationship Some
Chronic wasting disease of captive mule deer AND/OR elk Is a False Prion disease Inferred relationship Some
Bovine spongiform encephalopathy Is a False Prion disease Inferred relationship Some
Gerstmann-Straussler-Scheinker syndrome Is a True Prion disease Inferred relationship Some
Transmissible mink encephalopathy Is a False Prion disease Inferred relationship Some
Creutzfeldt-Jakob disease Is a True Prion disease Inferred relationship Some
Fatal familial insomnia Is a True Prion disease Inferred relationship Some
Kuru Is a False Prion disease Inferred relationship Some
Progressive subcortical gliosis Is a True Prion disease Inferred relationship Some
Cerebral degeneration due to Creutzfeldt-Jakob disease Is a False Prion disease Inferred relationship Some
[X]Dementia in Creutzfeldt-Jakob disease Is a False Prion disease Inferred relationship Some
Bovine spongiform encephalopathy Is a False Prion disease Inferred relationship Some
Prion disease associated with acquired immunodeficiency syndrome Is a False Prion disease Inferred relationship Some
Variant Creutzfeldt-Jakob disease (disorder) Is a True Prion disease Inferred relationship Some
Familial Alzheimer-like prion disease (disorder) Is a True Prion disease Inferred relationship Some
Variably protease sensitive prionopathy (disorder) Is a True Prion disease Inferred relationship Some
Acquired prion disease (disorder) Is a True Prion disease Inferred relationship Some
Prion protein systemic amyloidosis (disorder) Is a True Prion disease Inferred relationship Some
Dementia due to prion disease Due to True Prion disease Inferred relationship Some 2

This concept is not in any reference sets

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