FHIR IG analytics

Resources that use this resource

No resources found

Resources that this resource uses

Narrative

No narrative content found in resource

Source1

{
  "resourceType": "ValueSet",
  "id": "2.16.840.1.113762.1.4.1146.2154",
  "meta": {
    "versionId": "11",
    "lastUpdated": "2024-01-23T01:10:32.000-05:00",
    "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": "Congenital_Hypothyroidism,Trigger"
    },
    {
      "url": "http://hl7.org/fhir/StructureDefinition/resource-lastReviewDate",
      "valueDate": "2025-01-13"
    },
    {
      "url": "http://hl7.org/fhir/StructureDefinition/valueset-effectiveDate",
      "valueDate": "2024-01-23"
    }
  ],
  "url": "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1146.2154",
  "identifier": [
    {
      "system": "urn:ietf:rfc:3986",
      "value": "urn:oid:2.16.840.1.113762.1.4.1146.2154"
    }
  ],
  "version": "20240123",
  "name": "CongenitalHypothyroidismUnspecifiedDisordersSNOMED",
  "title": "Congenital Hypothyroidism [Unspecified] (Disorders) (SNOMED)",
  "status": "active",
  "date": "2024-01-23T01:10:32-05:00",
  "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 Congenital Hypothyroidism [Unspecified] regardless of the clinical presentation of the condition.),(Data Element Scope: Diagnoses or problems documented in a clinical record.),(Inclusion Criteria: Congenital Hypothyroidism [Unspecified]),(Exclusion Criteria: None)",
  "compose": {
    "include": [
      {
        "system": "http://snomed.info/sct",
        "concept": [
          {
            "code": "190268003",
            "display": "Congenital hypothyroidism (disorder)"
          },
          {
            "code": "206457007",
            "display": "Neonatal jaundice with congenital hypothyroidism (disorder)"
          },
          {
            "code": "237515009",
            "display": "Congenital hypothyroidism without goiter (disorder)"
          },
          {
            "code": "278503003",
            "display": "Congenital hypothyroidism with diffuse goiter (disorder)"
          },
          {
            "code": "722938007",
            "display": "Congenital central hypothyroidism (disorder)"
          },
          {
            "code": "770631009",
            "display": "Genetic transient congenital hypothyroidism (disorder)"
          },
          {
            "code": "771510006",
            "display": "X-linked central congenital hypothyroidism with late-onset testicular enlargement (disorder)"
          },
          {
            "code": "84781002",
            "display": "Sporadic cretinism (disorder)"
          }
        ]
      }
    ]
  },
  "expansion": {
    "identifier": "urn:uuid:250b5f01-1780-428e-80a9-6674c715a9a5",
    "timestamp": "2025-05-23T18:38:44-04:00",
    "total": 8,
    "contains": [
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "190268003",
        "display": "Congenital hypothyroidism (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "206457007",
        "display": "Neonatal jaundice with congenital hypothyroidism (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "237515009",
        "display": "Congenital hypothyroidism without goiter (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "278503003",
        "display": "Congenital hypothyroidism with diffuse goiter (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722938007",
        "display": "Congenital central hypothyroidism (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "770631009",
        "display": "Genetic transient congenital hypothyroidism (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "771510006",
        "display": "X-linked central congenital hypothyroidism with late-onset testicular enlargement (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "84781002",
        "display": "Sporadic cretinism (disorder)"
      }
    ]
  }
}