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Source1

{
  "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": "2025-01-13"
    },
    {
      "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:57f6faab-6bf3-4888-ba56-4e5c1046ba6b",
    "timestamp": "2025-05-23T18:23:32-04:00",
    "total": 7,
    "contains": [
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1003373003",
        "display": "Microcephaly with simplified gyral pattern (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1148757008",
        "display": "Microcephaly (finding)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1148758003",
        "display": "Congenital microcephaly (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "431265009",
        "display": "Fetal microcephaly (disorder)"
      },
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        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
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        "display": "Amish lethal microcephaly (disorder)"
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        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "715981004",
        "display": "Autosomal recessive primary microcephaly (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "78071008",
        "display": "Hydromicrocephaly (disorder)"
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    ]
  }
}