Resource ValueSet/FHIR Server from package us.nlm.vsac#0.22.0 (78 ms)

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	SNOMED codes used in this IG
http://snomed.info/sct	veri

Source

{
  "resourceType" : "ValueSet",
  "id" : "2.16.840.1.113762.1.4.1146.2502",
  "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,Trisomy13"
    },
    {
      "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/2.16.840.1.113762.1.4.1146.2502",
  "identifier" : [
    {
      "system" : "urn:ietf:rfc:3986",
      "value" : "urn:oid:2.16.840.1.113762.1.4.1146.2502"
    }
  ],
  "version" : "20250218",
  "name" : "Trisomy13DisordersSNOMED",
  "title" : "Trisomy 13 (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 13 regardless of the clinical presentation of the condition),(Data Element Scope: Diagnoses or problems documented in a clinical record.),(Inclusion Criteria: Trisomy 13),(Exclusion Criteria: none)",
  "compose" : {
    "include" : [
      {
        "system" : "http://snomed.info/sct",
        "concept" : [
          {
            "code" : "1003416001",
            "display" : "Medial duplication of chromosome 13 (disorder)"
          },
          {
            "code" : "1003909007",
            "display" : "Proximal duplication of chromosome 13 (disorder)"
          },
          {
            "code" : "10572007",
            "display" : "13q partial trisomy syndrome (disorder)"
          },
          {
            "code" : "125521000119101",
            "display" : "Fetus with complete trisomy 13 syndrome (disorder)"
          },
          {
            "code" : "205619006",
            "display" : "Trisomy 13, meiotic nondisjunction (disorder)"
          },
          {
            "code" : "205620000",
            "display" : "Trisomy 13 - mitotic nondisjunction mosaicism (disorder)"
          },
          {
            "code" : "21111006",
            "display" : "Complete trisomy 13 syndrome (disorder)"
          },
          {
            "code" : "254268004",
            "display" : "Partial trisomy 13 in Patau's syndrome (disorder)"
          },
          {
            "code" : "403756008",
            "display" : "Aplasia cutis in Trisomy 13 syndrome (disorder)"
          },
          {
            "code" : "548004",
            "display" : "13p partial trisomy syndrome (disorder)"
          },
          {
            "code" : "726352003",
            "display" : "Partial trisomy of chromosome 13 (disorder)"
          },
          {
            "code" : "737540008",
            "display" : "Trisomy 13 (morphologic abnormality)"
          },
          {
            "code" : "764454003",
            "display" : "Distal trisomy 13q (disorder)"
          },
          {
            "code" : "764996009",
            "display" : "Non-distal trisomy 13q (disorder)"
          },
          {
            "code" : "897549008",
            "display" : "Distal duplication of chromosome 13 (disorder)"
          }
        ]
      }
    ]
  },
  "expansion" : {
    "identifier" : "urn:uuid:77fa6576-e295-4d25-a83a-b6e6d2a4f2b2",
    "timestamp" : "2025-05-11T04:24:52-04:00",
    "total" : 15,
    "contains" : [
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        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20250301",
        "code" : "1003416001",
        "display" : "Medial duplication of chromosome 13 (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20250301",
        "code" : "1003909007",
        "display" : "Proximal duplication of chromosome 13 (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20250301",
        "code" : "10572007",
        "display" : "13q partial trisomy syndrome (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20250301",
        "code" : "125521000119101",
        "display" : "Fetus with complete trisomy 13 syndrome (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20250301",
        "code" : "205619006",
        "display" : "Trisomy 13, meiotic nondisjunction (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20250301",
        "code" : "205620000",
        "display" : "Trisomy 13 - mitotic nondisjunction mosaicism (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20250301",
        "code" : "21111006",
        "display" : "Complete trisomy 13 syndrome (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20250301",
        "code" : "254268004",
        "display" : "Partial trisomy 13 in Patau's syndrome (disorder)"
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      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20250301",
        "code" : "403756008",
        "display" : "Aplasia cutis in Trisomy 13 syndrome (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20250301",
        "code" : "548004",
        "display" : "13p partial trisomy syndrome (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20250301",
        "code" : "726352003",
        "display" : "Partial trisomy of chromosome 13 (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20250301",
        "code" : "737540008",
        "display" : "Trisomy 13 (morphologic abnormality)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20250301",
        "code" : "764454003",
        "display" : "Distal trisomy 13q (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20250301",
        "code" : "764996009",
        "display" : "Non-distal trisomy 13q (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20250301",
        "code" : "897549008",
        "display" : "Distal duplication of chromosome 13 (disorder)"
      }
    ]
  },
  "text" : {
  }
}

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