FHIR IG Statistics: ValueSet/2.16.840.1.113762.1.4.1146.2518

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{
  "resourceType": "ValueSet",
  "id": "2.16.840.1.113762.1.4.1146.2518",
  "meta": {
    "versionId": "6",
    "lastUpdated": "2025-02-18T01:09:30.000-05:00",
    "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": "Trigger,Trisomy_18"
    },
    {
      "url": "http://hl7.org/fhir/StructureDefinition/resource-lastReviewDate",
      "valueDate": "2025-02-18"
    },
    {
      "url": "http://hl7.org/fhir/StructureDefinition/valueset-effectiveDate",
      "valueDate": "2025-02-18"
    }
  ],
  "url": "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1146.2518",
  "identifier": [
    {
      "system": "urn:ietf:rfc:3986",
      "value": "urn:oid:2.16.840.1.113762.1.4.1146.2518"
    }
  ],
  "version": "20250218",
  "name": "Trisomy18DisordersSNOMED",
  "title": "Trisomy 18 (Disorders) (SNOMED)",
  "status": "active",
  "date": "2025-02-18T01:09:31-05:00",
  "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 Trisomy 18 regardless of the clinical presentation of the condition),(Data Element Scope: Diagnoses or problems documented in a clinical record.),(Inclusion Criteria: Trisomy 18),(Exclusion Criteria: none)",
  "compose": {
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            "display": "Trisomy 18 - meiotic nondisjunction (disorder)"
          },
          {
            "code": "205624009",
            "display": "Trisomy 18 - mitotic nondisjunction mosaicism (disorder)"
          },
          {
            "code": "254266000",
            "display": "Partial trisomy 18 in Edward's syndrome (disorder)"
          },
          {
            "code": "4199009",
            "display": "18p partial trisomy syndrome (disorder)"
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            "code": "51500006",
            "display": "Complete trisomy 18 syndrome (disorder)"
          },
          {
            "code": "66985009",
            "display": "18q partial trisomy syndrome (disorder)"
          },
          {
            "code": "726357009",
            "display": "Partial trisomy of chromosome 18 (disorder)"
          },
          {
            "code": "737541007",
            "display": "Trisomy 18 (morphologic abnormality)"
          },
          {
            "code": "782676009",
            "display": "Distal trisomy 18q (disorder)"
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        ]
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    ]
  },
  "expansion": {
    "identifier": "urn:uuid:cf62a0fe-1635-4764-8980-2c1092908dac",
    "timestamp": "2025-05-23T18:48:36-04:00",
    "total": 10,
    "contains": [
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        "system": "http://snomed.info/sct",
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        "version": "http://snomed.info/sct/731000124108/version/20250301",
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}