Resource ValueSet/FHIR Server from package us.nlm.vsac#0.21.0 (78 ms)

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" : "2.16.840.1.113762.1.4.1146.1095",
  "meta" : {
    "versionId" : "15",
    "lastUpdated" : "2024-01-22T01:09:37.000-05:00",
    "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" : "G_Common"
    },
    {
      "url" : "http://hl7.org/fhir/StructureDefinition/resource-lastReviewDate",
      "valueDate" : "2024-01-22"
    },
    {
      "url" : "http://hl7.org/fhir/StructureDefinition/valueset-effectiveDate",
      "valueDate" : "2024-01-22"
    }
  ],
  "url" : "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1146.1095",
  "identifier" : [
    {
      "system" : "urn:ietf:rfc:3986",
      "value" : "urn:oid:2.16.840.1.113762.1.4.1146.1095"
    }
  ],
  "version" : "20240122",
  "name" : "MicrocephalySNOMED",
  "title" : "Microcephaly (SNOMED)",
  "status" : "active",
  "date" : "2024-01-22T01:09:37-05:00",
  "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 microcephaly regardless of the clinical presentation of the condition),(Data Element Scope: Diagnoses or problems documented in a clinical record.),(Inclusion Criteria: Microcephaly),(Exclusion Criteria: Exclude codes that list multiple conditions, specific syndromes that include microcephaly (ex Feingold syndrome), and secondary disease.)",
  "compose" : {
    "include" : [
      {
        "system" : "http://snomed.info/sct",
        "concept" : [
          {
            "code" : "1003373003",
            "display" : "Microcephaly with simplified gyral pattern (disorder)"
          },
          {
            "code" : "1148757008",
            "display" : "Microcephaly (finding)"
          },
          {
            "code" : "1148758003",
            "display" : "Congenital microcephaly (disorder)"
          },
          {
            "code" : "1829003",
            "display" : "Microcephalus (disorder)"
          },
          {
            "code" : "431265009",
            "display" : "Fetal microcephaly (disorder)"
          },
          {
            "code" : "702437000",
            "display" : "Amish lethal microcephaly (disorder)"
          },
          {
            "code" : "715981004",
            "display" : "Autosomal recessive primary microcephaly (disorder)"
          },
          {
            "code" : "78071008",
            "display" : "Hydromicrocephaly (disorder)"
          }
        ]
      }
    ]
  },
  "expansion" : {
    "identifier" : "urn:uuid:01103fee-7175-4e38-91a8-3ccb74a962ae",
    "timestamp" : "2024-12-10T06:28:02-05:00",
    "total" : 7,
    "contains" : [
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "1003373003",
        "display" : "Microcephaly with simplified gyral pattern (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "1148757008",
        "display" : "Microcephaly (finding)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "1148758003",
        "display" : "Congenital microcephaly (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "431265009",
        "display" : "Fetal microcephaly (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "702437000",
        "display" : "Amish lethal microcephaly (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "715981004",
        "display" : "Autosomal recessive primary microcephaly (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "78071008",
        "display" : "Hydromicrocephaly (disorder)"
      }
    ]
  },
  "text" : {
  }
}

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