ValueSet-2.16.840.1.113762.1.4.1146.2137

Sourceus.nlm.vsac#0.11.0:null (v4.0.1)
resourceTypeValueSet
id2.16.840.1.113762.1.4.1146.2137
canonicalhttp://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1146.2137
version20230122
statusactive
publisherCSTE Steward
namePrionDiseaseDisordersSNOMED
titlePrion Disease (Disorders) (SNOMED)
date2023-01-22T01:03:33-05:00
Usages(none)

This value set contains 21 concepts

Code System Display
   1163119007 http://snomed.info/sct Creutzfeldt Jakob disease following graft of dura (disorder)
   1176989007 http://snomed.info/sct Parkinsonism due to prion disease (disorder)
   1177002007 http://snomed.info/sct Tic disorder due to prion disease (disorder)
   192818008 http://snomed.info/sct Cerebral degeneration due to Creutzfeldt-Jakob disease (disorder)
   20484008 http://snomed.info/sct Prion disease (disorder)
   304603007 http://snomed.info/sct Variant Creutzfeldt-Jakob disease (disorder)
   429458009 http://snomed.info/sct Dementia due to Creutzfeldt Jakob disease (disorder)
   67155006 http://snomed.info/sct Gerstmann-Straussler-Scheinker syndrome (disorder)
   713060000 http://snomed.info/sct Sporadic Creutzfeldt-Jakob disease (disorder)
   715662009 http://snomed.info/sct Iatrogenic Jakob-Creutzfeldt disease (disorder)
   715807002 http://snomed.info/sct Familial Creutzfeldt-Jakob (disorder)
   721165001 http://snomed.info/sct Variably protease sensitive prionopathy (disorder)
   721219005 http://snomed.info/sct Familial Alzheimer-like prion disease (disorder)
   721255002 http://snomed.info/sct Acquired prion disease (disorder)
   733422008 http://snomed.info/sct Prion protein systemic amyloidosis (disorder)
   762350007 http://snomed.info/sct Dementia due to prion disease (disorder)
   792004 http://snomed.info/sct Jakob-Creutzfeldt disease (disorder)
   83157008 http://snomed.info/sct Fatal familial insomnia (disorder)
   840452004 http://snomed.info/sct Classical sporadic Creutzfeldt-Jakob disease (disorder)
   860826006 http://snomed.info/sct Creutzfeldt-Jakob Disease caused by human growth hormone (disorder)
   86188000 http://snomed.info/sct Kuru (disorder)

Produced 08 Sep 2023