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Source1

{
  "resourceType": "ValueSet",
  "id": "2.16.840.1.113762.1.4.1146.2140",
  "meta": {
    "versionId": "6",
    "lastUpdated": "2023-12-21T17:43:03.000-05:00",
    "profile": [
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      "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": "Phenylketonuria,Trigger"
    },
    {
      "url": "http://hl7.org/fhir/StructureDefinition/resource-lastReviewDate",
      "valueDate": "2024-06-05"
    },
    {
      "url": "http://hl7.org/fhir/StructureDefinition/valueset-effectiveDate",
      "valueDate": "2023-01-22"
    }
  ],
  "url": "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1146.2140",
  "identifier": [
    {
      "system": "urn:ietf:rfc:3986",
      "value": "urn:oid:2.16.840.1.113762.1.4.1146.2140"
    }
  ],
  "version": "20230122",
  "name": "PhenylketonuriaDisordersSNOMED",
  "title": "Phenylketonuria (Disorders) (SNOMED)",
  "status": "active",
  "date": "2023-01-22T01:03:33-05:00",
  "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 Phenylketonuria regardless of the clinical presentation of the condition),(Data Element Scope: Diagnoses or problems documented in a clinical record.),(Inclusion Criteria: Phenylketonuria),(Exclusion Criteria: none)",
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          },
          {
            "code": "190687004",
            "display": "Phenylketonuria (disorder)"
          },
          {
            "code": "297225000",
            "display": "Maternal phenylketonuria (disorder)"
          },
          {
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          },
          {
            "code": "440009",
            "display": "Persistent hyperphenylalaninemia (disorder)"
          },
          {
            "code": "60590005",
            "display": "Maternal phenylketonuria fetal effect (disorder)"
          },
          {
            "code": "7573000",
            "display": "Classical phenylketonuria (disorder)"
          },
          {
            "code": "890435004",
            "display": "Classical phenylketonuria with partial deficiency of phenylalanine hydroxylase (disorder)"
          },
          {
            "code": "890436003",
            "display": "Classical phenylketonuria with total deficiency of phenylalanine hydroxylase (disorder)"
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        ]
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  "expansion": {
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    "timestamp": "2025-05-23T18:38:20-04:00",
    "total": 8,
    "contains": [
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}