FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.4.11  |  FHIR Version n/a  User: [n/a]

Resource ValueSet/FHIR Server from package us.nlm.vsac#0.21.0 (219 ms)

Package us.nlm.vsac
Type ValueSet
Id Id
FHIR Version R4
Source http://fhir.org/packages/us.nlm.vsac/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)
Experimental False
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)

Resources that use this resource

No resources found

Resources that this resource uses

CodeSystem
http://snomed.info/sct SNOMED CT (all versions)
http://snomed.info/sct Nutrition Care Process Terminology module
http://snomed.info/sct veri

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" : "2024-01-23"
    },
    {
      "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:7a791027-0cfa-432a-9937-bf7ae1342e9e",
    "timestamp" : "2024-12-10T06:50:20-05:00",
    "total" : 29,
    "contains" : [
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "1163119007",
        "display" : "Creutzfeldt Jakob disease following graft of dura (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "1176989007",
        "display" : "Parkinsonism due to prion disease (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "1177002007",
        "display" : "Tic disorder due to prion disease (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "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/20240901",
        "code" : "1259478009",
        "display" : "Dementia due to familial Creutzfeldt-Jakob disease (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "1259480003",
        "display" : "Dementia due to fatal familial insomnia (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "1259501004",
        "display" : "Dementia due to kuru (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "1259503001",
        "display" : "Dementia due to iatrogenic Creutzfeldt-Jakob disease (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "1259522005",
        "display" : "Dementia due to variant Creutzfeldt-Jakob disease (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "1259529001",
        "display" : "Dementia due to sporadic Creutzfeldt-Jakob disease (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "1259640001",
        "display" : "Chorea due to prion disease (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "192818008",
        "display" : "Cerebral degeneration due to Creutzfeldt-Jakob disease (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "20484008",
        "display" : "Prion disease (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "304603007",
        "display" : "Variant Creutzfeldt-Jakob disease (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "429458009",
        "display" : "Dementia due to Creutzfeldt Jakob disease (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "67155006",
        "display" : "Gerstmann-Straussler-Scheinker syndrome (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "713060000",
        "display" : "Sporadic Creutzfeldt-Jakob disease (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "715662009",
        "display" : "Iatrogenic Jakob-Creutzfeldt disease (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "715807002",
        "display" : "Familial Creutzfeldt-Jakob (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "721165001",
        "display" : "Variably protease sensitive prionopathy (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "721219005",
        "display" : "Familial Alzheimer-like prion disease (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "721255002",
        "display" : "Acquired prion disease (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "733422008",
        "display" : "Prion protein systemic amyloidosis (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "762350007",
        "display" : "Dementia due to prion disease (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "792004",
        "display" : "Jakob-Creutzfeldt disease (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "83157008",
        "display" : "Fatal familial insomnia (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "840452004",
        "display" : "Classical sporadic Creutzfeldt-Jakob disease (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "860826006",
        "display" : "Creutzfeldt-Jakob Disease caused by human growth hormone (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "86188000",
        "display" : "Kuru (disorder)"
      }
    ]
  },
  "text" : {
  }
}

XIG built as of ??metadata-date??. Found ??metadata-resources?? resources in ??metadata-packages?? packages.