{
  "description": null,
  "compose": {
    "include": [ {
      "system": "http://snomed.info/sct",
      "concept": [ {
        "code": "127037003",
        "display": "Toxic methemoglobinemia with cyanosis (disorder)"
      }, {
        "code": "131171006",
        "display": "Increased methemoglobin (finding)"
      }, {
        "code": "191388008",
        "display": "Familial methemoglobinemia (disorder)"
      }, {
        "code": "191389000",
        "display": "Idiopathic methemoglobinemia (disorder)"
      }, {
        "code": "191390009",
        "display": "Drug-induced methemoglobinemia (disorder)"
      }, {
        "code": "234395000",
        "display": "Congenital methemoglobinaema with defective methemoglobin-reducing system (disorder)"
      }, {
        "code": "234396004",
        "display": "Congenital methemoglobinemia with abnormal methemoglobins (disorder)"
      }, {
        "code": "267550008",
        "display": "Congenital methemoglobinemia (disorder)"
      }, {
        "code": "295315008",
        "display": "Acquired methemoglobinemia (disorder)"
      }, {
        "code": "38959009",
        "display": "Methemoglobinemia (disorder)"
      }, {
        "code": "406593009",
        "display": "Methemoglobinemia caused by nitrate poisoning (disorder)"
      }, {
        "code": "57020009",
        "display": "Stokvis' disease (disorder)"
      }, {
        "code": "74912001",
        "display": "Hereditary methemoglobinemia due to globin chain mutation (disorder)"
      }, {
        "code": "767497003",
        "display": "Autosomal recessive congenital methemoglobinemia (disorder)"
      }, {
        "code": "767498008",
        "display": "Autosomal recessive congenital methemoglobinemia type II (disorder)"
      }, {
        "code": "767499000",
        "display": "Autosomal recessive congenital methemoglobinemia type I (disorder)"
      } ]
    } ]
  },
  "_filename": "ValueSet-2.16.840.1.113762.1.4.1146.2105.json",
  "package_name": "us.nlm.vsac",
  "date": "2023-01-25T01:08:07-05:00",
  "meta": {
    "profile": [ "http://hl7.org/fhir/StructureDefinition/shareablevalueset", "http://hl7.org/fhir/us/cqfmeasures/StructureDefinition/publishable-valueset-cqfm" ],
    "versionId": "7",
    "lastUpdated": "2023-01-25T01:08:07.000-05:00"
  },
  "publisher": "CSTE Steward",
  "jurisdiction": [ {
    "extension": [ {
      "url": "http://hl7.org/fhir/StructureDefinition/data-absent-reason",
      "valueCode": "unknown"
    } ]
  } ],
  "purpose": "(Clinical Focus: This set of values contains diagnoses or problems that represent that the patient has Methemoglobinemia regardless of the clinical presentation of the condition),(Data Element Scope: Diagnoses or problems documented in a clinical record.),(Inclusion Criteria: Methemoglobinemia),(Exclusion Criteria: None)",
  "name": "MethemoglobinemiaDisordersSNOMED",
  "type": null,
  "experimental": null,
  "resourceType": "ValueSet",
  "expansion": {
    "total": 16,
    "offset": 0,
    "contains": [ {
      "code": "127037003",
      "system": "http://snomed.info/sct",
      "display": "Toxic methemoglobinemia with cyanosis (disorder)",
      "version": "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "code": "131171006",
      "system": "http://snomed.info/sct",
      "display": "Methemoglobin above reference range (finding)",
      "version": "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "code": "191388008",
      "system": "http://snomed.info/sct",
      "display": "Familial methemoglobinemia (disorder)",
      "version": "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "code": "191389000",
      "system": "http://snomed.info/sct",
      "display": "Idiopathic methemoglobinemia (disorder)",
      "version": "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "code": "191390009",
      "system": "http://snomed.info/sct",
      "display": "Drug-induced methemoglobinemia (disorder)",
      "version": "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "code": "234395000",
      "system": "http://snomed.info/sct",
      "display": "Congenital methemoglobinaema with defective methemoglobin-reducing system (disorder)",
      "version": "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "code": "234396004",
      "system": "http://snomed.info/sct",
      "display": "Congenital methemoglobinemia with abnormal methemoglobins (disorder)",
      "version": "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "code": "267550008",
      "system": "http://snomed.info/sct",
      "display": "Congenital methemoglobinemia (disorder)",
      "version": "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "code": "295315008",
      "system": "http://snomed.info/sct",
      "display": "Acquired methemoglobinemia (disorder)",
      "version": "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "code": "38959009",
      "system": "http://snomed.info/sct",
      "display": "Methemoglobinemia (disorder)",
      "version": "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "code": "406593009",
      "system": "http://snomed.info/sct",
      "display": "Methemoglobinemia caused by nitrate poisoning (disorder)",
      "version": "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "code": "57020009",
      "system": "http://snomed.info/sct",
      "display": "Stokvis' disease (disorder)",
      "version": "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "code": "74912001",
      "system": "http://snomed.info/sct",
      "display": "Hereditary methemoglobinemia due to globin chain mutation (disorder)",
      "version": "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "code": "767497003",
      "system": "http://snomed.info/sct",
      "display": "Autosomal recessive congenital methemoglobinemia (disorder)",
      "version": "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "code": "767498008",
      "system": "http://snomed.info/sct",
      "display": "Autosomal recessive congenital methemoglobinemia type II (disorder)",
      "version": "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "code": "767499000",
      "system": "http://snomed.info/sct",
      "display": "Autosomal recessive congenital methemoglobinemia type I (disorder)",
      "version": "http://snomed.info/sct/731000124108/version/20230901"
    } ],
    "parameter": [ {
      "name": "count",
      "valueInteger": 1000
    }, {
      "name": "offset",
      "valueInteger": 0
    } ],
    "timestamp": "2023-10-19T19:24:27-04:00",
    "identifier": "urn:uuid:5bc772da-b0d4-462e-a49a-d878a059f1fe"
  },
  "title": "Methemoglobinemia (Disorders) (SNOMED)",
  "package_version": "0.13.0",
  "extension": [ {
    "url": "http://hl7.org/fhir/StructureDefinition/valueset-author",
    "valueString": "CSTE Author"
  }, {
    "url": "http://hl7.org/fhir/StructureDefinition/valueset-keyWord",
    "valueString": "Methemoglobinemia,Trigger"
  }, {
    "url": "http://hl7.org/fhir/StructureDefinition/resource-lastReviewDate",
    "valueDate": "2023-01-25"
  }, {
    "url": "http://hl7.org/fhir/StructureDefinition/valueset-effectiveDate",
    "valueDate": "2023-01-25"
  } ],
  "status": "active",
  "id": "ab728dbd-1cfd-485b-a794-2c079ed4cba5",
  "kind": null,
  "url": "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1146.2105",
  "identifier": [ {
    "value": "urn:oid:2.16.840.1.113762.1.4.1146.2105",
    "system": "urn:ietf:rfc:3986"
  } ],
  "version": "20230125"
}