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Source1

{
  "resourceType": "ValueSet",
  "id": "1.3.6.1.4.1.19376.1.7.3.1.1.13.8.61",
  "meta": {
    "source": "https://phinvads.cdc.gov/vads/ViewValueSet.action?oid=1.3.6.1.4.1.19376.1.7.3.1.1.13.8.61"
  },
  "url": "http://phinvads.cdc.gov/fhir/ValueSet/1.3.6.1.4.1.19376.1.7.3.1.1.13.8.61",
  "version": "2",
  "name": "PHVS_DownSyndrome_NCHS",
  "title": "Down Syndrome (NCHS)",
  "status": "active",
  "date": "2014-01-22T00:09:00+11:00",
  "description": "To reflect Down Syndrome as an anomaly of the newborn",
  "compose": {
    "include": [
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20200901",
        "concept": [
          {
            "code": "70156005",
            "display": "Anomaly of chromosome pair 21"
          },
          {
            "code": "41040004",
            "display": "Complete trisomy 21 syndrome"
          },
          {
            "code": "205615000",
            "display": "Trisomy 21- meiotic nondisjunction"
          },
          {
            "code": "205616004",
            "display": "Trisomy 21- mitotic nondisjunction mosaicism"
          },
          {
            "code": "254264002",
            "display": "Partial trisomy 21 in Down's syndrome"
          },
          {
            "code": "371045000",
            "display": "Translocation Down syndrome"
          }
        ]
      }
    ]
  }
}