FHIR IG analytics| Package | us.nlm.vsac |
| Resource Type | ValueSet |
| Id | ValueSet-2.16.840.1.113762.1.4.1146.2137.json |
| FHIR Version | R4 |
| Source | https://vsac.nlm.nih.gov/valueset/2.16.840.1.113762.1.4.1146.2137/expansion |
| URL | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1146.2137 |
| Version | 20240123 |
| Status | active |
| Date | 2024-01-23T01:10:32-05:00 |
| Name | PrionDiseaseDisordersSNOMED |
| Title | Prion Disease (Disorders) (SNOMED) |
| Realm | us |
| Authority | hl7 |
| Purpose | (Clinical Focus: This set of values contains diagnoses or problems that represent that the patient has Prion Disease regardless of the clinical presentation of the condition),(Data Element Scope: Diagnoses or problems documented in a clinical record.),(Inclusion Criteria: Prion Disease),(Exclusion Criteria: none) |
No resources found
| CodeSystem | |
| sct | SNOMED codes used in this IG |
No narrative content found in resource
FHIR
FHIRsmith{
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"title": "Prion Disease (Disorders) (SNOMED)",
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"date": "2024-01-23T01:10:32-05:00",
"publisher": "CSTE Steward",
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"compose": {
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"display": "Creutzfeldt Jakob disease following graft of dura (disorder)"
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{
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{
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"display": "Gerstmann-Straussler-Scheinker syndrome (disorder)"
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"display": "Sporadic Creutzfeldt-Jakob disease (disorder)"
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"display": "Iatrogenic Jakob-Creutzfeldt disease (disorder)"
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{
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"display": "Familial Creutzfeldt-Jakob (disorder)"
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{
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"display": "Variably protease sensitive prionopathy (disorder)"
},
{
"code": "721219005",
"display": "Familial Alzheimer-like prion disease (disorder)"
},
{
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{
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"display": "Prion protein systemic amyloidosis (disorder)"
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{
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"display": "Dementia due to prion disease (disorder)"
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"display": "Jakob-Creutzfeldt disease (disorder)"
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{
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"display": "Fatal familial insomnia (disorder)"
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{
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"display": "Classical sporadic Creutzfeldt-Jakob disease (disorder)"
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{
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