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Resource ValueSet/FHIR Server from package us.nlm.vsac#0.21.0 (125 ms)

Package us.nlm.vsac
Type ValueSet
Id Id
FHIR Version R4
Source http://fhir.org/packages/us.nlm.vsac/https://vsac.nlm.nih.gov/valueset/2.16.840.1.113762.1.4.1146.2153/expansion
Url http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1146.2153
Version 20240123
Status active
Date 2024-01-23T01:10:32-05:00
Name PrimaryCongenitalHypothyroidismDisordersSNOMED
Title Primary Congenital Hypothyroidism (Disorders) (SNOMED)
Experimental False
Realm us
Authority hl7
Purpose (Clinical Focus: This set of values contains diagnoses or problems that represent that the patient has Primary Congenital Hypothyroidism regardless of the clinical presentation of the condition.),(Data Element Scope: Diagnoses or problems documented in a clinical record.),(Inclusion Criteria: Primary Congenital Hypothyroidism.),(Exclusion Criteria: None)

Resources that use this resource

No resources found

Resources that this resource uses

CodeSystem
http://snomed.info/sct SNOMED CT (all versions)
http://snomed.info/sct Nutrition Care Process Terminology module
http://snomed.info/sct veri

Source

{
  "resourceType" : "ValueSet",
  "id" : "2.16.840.1.113762.1.4.1146.2153",
  "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" : "Primary_Congenital_Hypothyroidism,Trigger"
    },
    {
      "url" : "http://hl7.org/fhir/StructureDefinition/resource-lastReviewDate",
      "valueDate" : "2024-01-23"
    },
    {
      "url" : "http://hl7.org/fhir/StructureDefinition/valueset-effectiveDate",
      "valueDate" : "2024-01-23"
    }
  ],
  "url" : "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1146.2153",
  "identifier" : [
    {
      "system" : "urn:ietf:rfc:3986",
      "value" : "urn:oid:2.16.840.1.113762.1.4.1146.2153"
    }
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  "version" : "20240123",
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  "title" : "Primary Congenital Hypothyroidism (Disorders) (SNOMED)",
  "status" : "active",
  "date" : "2024-01-23T01:10:32-05:00",
  "publisher" : "CSTE Steward",
  "jurisdiction" : [
    {
      "coding" : [
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          "system" : "urn:iso:std:iso:3166",
          "code" : "US"
        }
      ]
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          {
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          {
            "code" : "1179401002",
            "display" : "Congenital hypothyroidism due to peripheral resistance to thyroid hormone (disorder)"
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          },
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          {
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            "display" : "Congenital hypothyroidism with ectopic thyroid (disorder)"
          },
          {
            "code" : "22558005",
            "display" : "Iodide transport defect (disorder)"
          },
          {
            "code" : "237555006",
            "display" : "Hypothyroidism due to iodide trapping defect (disorder)"
          },
          {
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            "display" : "Iodide oxidation defect (disorder)"
          },
          {
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          },
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            "display" : "Choreoathetosis with congenital hypothyroidism and neonatal respiratory distress syndrome (disorder)"
          },
          {
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            "display" : "Bamforth Lazarus syndrome (disorder)"
          },
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            "display" : "Congenital hypothyroidism due to iodine deficiency (disorder)"
          },
          {
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          },
          {
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          },
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        "code" : "722375007",
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      {
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        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "722939004",
        "display" : "Congenital hypothyroidism due to iodine deficiency (disorder)"
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      {
        "system" : "http://snomed.info/sct",
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        "code" : "725462002",
        "display" : "Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "783177006",
        "display" : "Congenital hypothyroidism due to maternal intake of antithyroid drug (disorder)"
      }
    ]
  },
  "text" : {
  }
}

XIG built as of ??metadata-date??. Found ??metadata-resources?? resources in ??metadata-packages?? packages.