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Source1

{
  "resourceType": "ValueSet",
  "id": "2.16.840.1.114222.4.11.7608",
  "meta": {
    "source": "https://phinvads.cdc.gov/vads/ViewValueSet.action?oid=2.16.840.1.114222.4.11.7608"
  },
  "url": "http://phinvads.cdc.gov/fhir/ValueSet/2.16.840.1.114222.4.11.7608",
  "version": "4",
  "name": "PHVS_Complications_CRS",
  "title": "Type Of Complication (CRS)",
  "status": "active",
  "date": "2017-01-25T00:10:00+11:00",
  "description": "Complications associated with the illness being reported",
  "compose": {
    "include": [
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20200901",
        "concept": [
          {
            "code": "128306009",
            "display": "Cataract"
          },
          {
            "code": "15188001",
            "display": "Hearing Impairment"
          },
          {
            "code": "13213009",
            "display": "Congenital heart disease"
          },
          {
            "code": "83330001",
            "display": "Patent ductus arteriosus"
          },
          {
            "code": "415582006",
            "display": "Stenosis"
          },
          {
            "code": "204113001",
            "display": "Congenital glaucoma"
          },
          {
            "code": "13225007",
            "display": "Meningoencephalitis"
          },
          {
            "code": "12393003",
            "display": "Purpura"
          },
          {
            "code": "16294009",
            "display": "Enlarged spleen"
          },
          {
            "code": "80515008",
            "display": "Enlarged liver"
          },
          {
            "code": "387712008",
            "display": "Neonatal jaundice"
          }
        ]
      },
      {
        "system": "urn:oid:2.16.840.1.114222.4.5.232",
        "version": "20200528",
        "concept": [
          {
            "code": "CRS021",
            "display": "Other congenital heart disease, specify"
          },
          {
            "code": "INV345",
            "display": "Peripheral pulmonic stenosis"
          },
          {
            "code": "INV347",
            "display": "Pigmentary retinopathy"
          },
          {
            "code": "INV348",
            "display": "Developmental delay or Mental retardation"
          },
          {
            "code": "INV350",
            "display": "Microencephaly"
          },
          {
            "code": "INV354",
            "display": "Radiolucent bone disease"
          },
          {
            "code": "INV356",
            "display": "Low platelets"
          },
          {
            "code": "INV357",
            "display": "Dermal erythropoieses (Blueberry Muffin Syndrome)"
          }
        ]
      },
      {
        "system": "http://terminology.hl7.org/CodeSystem/v3-NullFlavor",
        "version": "20090501",
        "concept": [
          {
            "code": "OTH",
            "display": "Other"
          },
          {
            "code": "UNK",
            "display": "Unknown"
          }
        ]
      }
    ]
  }
}