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Packageus.nlm.vsac
Resource TypeValueSet
IdValueSet-2.16.840.1.113762.1.4.1146.1337.json
FHIR VersionR4
Sourcehttps://vsac.nlm.nih.gov/valueset/2.16.840.1.113762.1.4.1146.1337/expansion
URLhttp://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1146.1337
Version20240620
Statusactive
Date2024-06-20T01:22:57-04:00
NameVariantCreutzfeldtJakobDiseaseDisordersSNOMED
TitleVariant Creutzfeldt Jakob Disease (Disorders) (SNOMED)
Realmus
Authorityhl7
Purpose(Clinical Focus: This set of values contains diagnoses or problems that represent that the patient has Variant Creutzfeldt Jakob Disease regardless of the clinical presentation of the clinical presentation of the condition.),(Data Element Scope: Diagnoses or problems documented in a clinical record.),(Inclusion Criteria: Variant Creutzfeldt Jakob Disease),(Exclusion Criteria: none)

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Resources that this resource uses

CodeSystem
sctSNOMED codes used in this IG

Narrative

No narrative content found in resource


Source1

{
  "resourceType": "ValueSet",
  "id": "2.16.840.1.113762.1.4.1146.1337",
  "meta": {
    "versionId": "11",
    "lastUpdated": "2024-06-20T01:22:57.000-04:00",
    "profile": [
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      "http://hl7.org/fhir/us/cqfmeasures/StructureDefinition/computable-valueset-cqfm",
      "http://hl7.org/fhir/us/cqfmeasures/StructureDefinition/publishable-valueset-cqfm"
    ]
  },
  "extension": [
    {
      "url": "http://hl7.org/fhir/StructureDefinition/valueset-author",
      "valueContactDetail": {
        "name": "CSTE Author"
      }
    },
    {
      "url": "http://hl7.org/fhir/StructureDefinition/valueset-keyWord",
      "valueString": "Prion_Disease,Trigger"
    },
    {
      "url": "http://hl7.org/fhir/StructureDefinition/resource-lastReviewDate",
      "valueDate": "2024-06-20"
    },
    {
      "url": "http://hl7.org/fhir/StructureDefinition/valueset-effectiveDate",
      "valueDate": "2024-06-20"
    }
  ],
  "url": "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1146.1337",
  "identifier": [
    {
      "system": "urn:ietf:rfc:3986",
      "value": "urn:oid:2.16.840.1.113762.1.4.1146.1337"
    }
  ],
  "version": "20240620",
  "name": "VariantCreutzfeldtJakobDiseaseDisordersSNOMED",
  "title": "Variant Creutzfeldt Jakob Disease (Disorders) (SNOMED)",
  "status": "active",
  "date": "2024-06-20T01:22:57-04:00",
  "publisher": "CSTE Steward",
  "jurisdiction": [
    {
      "coding": [
        {
          "system": "urn:iso:std:iso:3166",
          "code": "US"
        }
      ]
    }
  ],
  "purpose": "(Clinical Focus: This set of values contains diagnoses or problems that represent that the patient has Variant Creutzfeldt Jakob Disease regardless of the clinical presentation of the clinical presentation of the condition.),(Data Element Scope: Diagnoses or problems documented in a clinical record.),(Inclusion Criteria: Variant Creutzfeldt Jakob Disease),(Exclusion Criteria: none)",
  "compose": {
    "include": [
      {
        "system": "http://snomed.info/sct",
        "concept": [
          {
            "code": "1259522005",
            "display": "Dementia due to variant Creutzfeldt-Jakob disease (disorder)"
          },
          {
            "code": "304603007",
            "display": "Variant Creutzfeldt-Jakob disease (disorder)"
          }
        ]
      }
    ]
  },
  "expansion": {
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    "timestamp": "2025-05-23T18:25:50-04:00",
    "total": 2,
    "contains": [
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        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259522005",
        "display": "Dementia due to variant Creutzfeldt-Jakob disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "304603007",
        "display": "Variant Creutzfeldt-Jakob disease (disorder)"
      }
    ]
  }
}