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FHIR IG Statistics: ValueSet/2.16.840.1.113762.1.4.1146.2137

Packageus.nlm.vsac
Resource TypeValueSet
Id2.16.840.1.113762.1.4.1146.2137
FHIR VersionR4
Sourcehttp://fhir.org/packages/us.nlm.vsac/https://vsac.nlm.nih.gov/valueset/2.16.840.1.113762.1.4.1146.2137/expansion
URLhttp://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1146.2137
Version20240123
Statusactive
Date2024-01-23T01:10:32-05:00
NamePrionDiseaseDisordersSNOMED
TitlePrion Disease (Disorders) (SNOMED)
Realmus
Authorityhl7
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)

Resources that use this resource

No resources found

Resources that this resource uses

CodeSystem
sctSNOMED CT (all versions)

Narrative

No narrative content found in resource

Source

{
  "resourceType": "ValueSet",
  "id": "2.16.840.1.113762.1.4.1146.2137",
  "meta": {
    "versionId": "11",
    "lastUpdated": "2024-01-23T01:10:32.000-05:00",
    "profile": [
      "http://hl7.org/fhir/StructureDefinition/shareablevalueset",
      "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": "2025-01-13"
    },
    {
      "url": "http://hl7.org/fhir/StructureDefinition/valueset-effectiveDate",
      "valueDate": "2024-01-23"
    }
  ],
  "url": "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1146.2137",
  "identifier": [
    {
      "system": "urn:ietf:rfc:3986",
      "value": "urn:oid:2.16.840.1.113762.1.4.1146.2137"
    }
  ],
  "version": "20240123",
  "name": "PrionDiseaseDisordersSNOMED",
  "title": "Prion Disease (Disorders) (SNOMED)",
  "status": "active",
  "date": "2024-01-23T01:10:32-05:00",
  "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 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)",
  "compose": {
    "include": [
      {
        "system": "http://snomed.info/sct",
        "concept": [
          {
            "code": "1163119007",
            "display": "Creutzfeldt Jakob disease following graft of dura (disorder)"
          },
          {
            "code": "1176989007",
            "display": "Parkinsonism due to prion disease (disorder)"
          },
          {
            "code": "1177002007",
            "display": "Tic disorder due to prion disease (disorder)"
          },
          {
            "code": "1259081008",
            "display": "Disorder of autonomic nervous system due to prion disease (disorder)"
          },
          {
            "code": "1259478009",
            "display": "Dementia due to familial Creutzfeldt-Jakob disease (disorder)"
          },
          {
            "code": "1259480003",
            "display": "Dementia due to fatal familial insomnia (disorder)"
          },
          {
            "code": "1259501004",
            "display": "Dementia due to kuru (disorder)"
          },
          {
            "code": "1259503001",
            "display": "Dementia due to iatrogenic Creutzfeldt-Jakob disease (disorder)"
          },
          {
            "code": "1259522005",
            "display": "Dementia due to variant Creutzfeldt-Jakob disease (disorder)"
          },
          {
            "code": "1259529001",
            "display": "Dementia due to sporadic Creutzfeldt-Jakob disease (disorder)"
          },
          {
            "code": "1259640001",
            "display": "Chorea due to prion disease (disorder)"
          },
          {
            "code": "192818008",
            "display": "Cerebral degeneration due to Creutzfeldt-Jakob disease (disorder)"
          },
          {
            "code": "20484008",
            "display": "Prion disease (disorder)"
          },
          {
            "code": "304603007",
            "display": "Variant Creutzfeldt-Jakob disease (disorder)"
          },
          {
            "code": "429458009",
            "display": "Dementia due to Creutzfeldt Jakob disease (disorder)"
          },
          {
            "code": "67155006",
            "display": "Gerstmann-Straussler-Scheinker syndrome (disorder)"
          },
          {
            "code": "713060000",
            "display": "Sporadic Creutzfeldt-Jakob disease (disorder)"
          },
          {
            "code": "715662009",
            "display": "Iatrogenic Jakob-Creutzfeldt disease (disorder)"
          },
          {
            "code": "715807002",
            "display": "Familial Creutzfeldt-Jakob (disorder)"
          },
          {
            "code": "721165001",
            "display": "Variably protease sensitive prionopathy (disorder)"
          },
          {
            "code": "721219005",
            "display": "Familial Alzheimer-like prion disease (disorder)"
          },
          {
            "code": "721255002",
            "display": "Acquired prion disease (disorder)"
          },
          {
            "code": "733422008",
            "display": "Prion protein systemic amyloidosis (disorder)"
          },
          {
            "code": "762350007",
            "display": "Dementia due to prion disease (disorder)"
          },
          {
            "code": "792004",
            "display": "Jakob-Creutzfeldt disease (disorder)"
          },
          {
            "code": "83157008",
            "display": "Fatal familial insomnia (disorder)"
          },
          {
            "code": "840452004",
            "display": "Classical sporadic Creutzfeldt-Jakob disease (disorder)"
          },
          {
            "code": "860826006",
            "display": "Creutzfeldt-Jakob Disease caused by human growth hormone (disorder)"
          },
          {
            "code": "86188000",
            "display": "Kuru (disorder)"
          }
        ]
      }
    ]
  },
  "expansion": {
    "identifier": "urn:uuid:76a9d888-22bb-4f86-ba16-8f2a57510cf5",
    "timestamp": "2025-05-23T18:38:15-04:00",
    "total": 29,
    "contains": [
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1163119007",
        "display": "Creutzfeldt Jakob disease following graft of dura (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1176989007",
        "display": "Parkinsonism due to prion disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1177002007",
        "display": "Tic disorder due to prion disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259081008",
        "display": "Disorder of autonomic nervous system due to prion disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259478009",
        "display": "Dementia due to familial Creutzfeldt-Jakob disease (disorder)"
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      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259480003",
        "display": "Dementia due to fatal familial insomnia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259501004",
        "display": "Dementia due to kuru (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259503001",
        "display": "Dementia due to iatrogenic Creutzfeldt-Jakob disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259522005",
        "display": "Dementia due to variant Creutzfeldt-Jakob disease (disorder)"
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        "version": "http://snomed.info/sct/731000124108/version/20250301",
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        "system": "http://snomed.info/sct",
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        "display": "Chorea due to prion disease (disorder)"
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        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "192818008",
        "display": "Cerebral degeneration due to Creutzfeldt-Jakob disease (disorder)"
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        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "20484008",
        "display": "Prion disease (disorder)"
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        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "304603007",
        "display": "Variant Creutzfeldt-Jakob disease (disorder)"
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        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "429458009",
        "display": "Dementia due to Creutzfeldt Jakob disease (disorder)"
      },
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        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "67155006",
        "display": "Gerstmann-Straussler-Scheinker syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "713060000",
        "display": "Sporadic Creutzfeldt-Jakob disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "715662009",
        "display": "Iatrogenic Jakob-Creutzfeldt disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "715807002",
        "display": "Familial Creutzfeldt-Jakob (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "721165001",
        "display": "Variably protease sensitive prionopathy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "721219005",
        "display": "Familial Alzheimer-like prion disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "721255002",
        "display": "Acquired prion disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "733422008",
        "display": "Prion protein systemic amyloidosis (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "762350007",
        "display": "Dementia due to prion disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "792004",
        "display": "Jakob-Creutzfeldt disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "83157008",
        "display": "Fatal familial insomnia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "840452004",
        "display": "Classical sporadic Creutzfeldt-Jakob disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "860826006",
        "display": "Creutzfeldt-Jakob Disease caused by human growth hormone (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "86188000",
        "display": "Kuru (disorder)"
      }
    ]
  }
}