{
"description": "documented diagnosis of Thalassemia (Business ID: Entry 3640047)",
"compose": {
"include": [ {
"filter": [ {
"op": "is-a",
"value": "40108008",
"property": "concept"
} ],
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20230901"
} ]
},
"_filename": "ValueSet-2.16.840.1.113762.1.4.1222.772.json",
"package_name": "us.nlm.vsac",
"date": "2021-09-16T01:01:06-04:00",
"meta": {
"profile": [ "http://hl7.org/fhir/StructureDefinition/shareablevalueset", "http://hl7.org/fhir/us/cqfmeasures/StructureDefinition/publishable-valueset-cqfm" ],
"versionId": "5",
"lastUpdated": "2021-09-16T01:01:06.000-04:00"
},
"publisher": "HL7 Patient Care WG Steward",
"jurisdiction": [ {
"coding": [ {
"code": "US",
"system": "urn:iso:std:iso:3166"
} ]
} ],
"purpose": "(Clinical Focus: This set of values addresses terms representing Thalassemia.),(Data Element Scope: The intent of this set of values is to identify patients who have a/an documented diagnosis of thalassemia.),(Inclusion Criteria: Includes SNOMEDCT codes for Thalassemia.),(Exclusion Criteria: Terms not representative of observable encoded terms that may have values indicating Thalassemia.)",
"name": "Thalassemia",
"type": null,
"experimental": "false",
"resourceType": "ValueSet",
"expansion": {
"total": 73,
"contains": [ {
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"display": "Thalassemia in mother complicating childbirth (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
"code": "111572002",
"system": "http://snomed.info/sct",
"display": "Beta zero thalassemia non deletion type (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
"code": "1148897000",
"system": "http://snomed.info/sct",
"display": "Hemoglobin Paksé disease (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
"code": "1148899002",
"system": "http://snomed.info/sct",
"display": "Hemoglobin Seal Rock disease (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
"code": "119641000119103",
"system": "http://snomed.info/sct",
"display": "Homozygous hemoglobin H constant spring thalassemia (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
"code": "119691000119106",
"system": "http://snomed.info/sct",
"display": "Hemoglobin C/beta thalassemia disease (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
"code": "119701000119106",
"system": "http://snomed.info/sct",
"display": "Hemoglobin D/beta thalassemia disease (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
"code": "127041004",
"system": "http://snomed.info/sct",
"display": "Sickle cell-beta-thalassemia (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
"code": "127042006",
"system": "http://snomed.info/sct",
"display": "Sickle cell beta plus thalassemia (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
"code": "127043001",
"system": "http://snomed.info/sct",
"display": "Sickle cell-beta^0^-thalassemia (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
"code": "127044007",
"system": "http://snomed.info/sct",
"display": "Sickle cell-delta beta^0^-thalassemia (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
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"system": "http://snomed.info/sct",
"display": "Sickle cell anemia with coexistent alpha-thalassemia (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
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"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
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"display": "Delta beta thalassemia (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
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"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
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}, {
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"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
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"version": "http://snomed.info/sct/731000124108/version/20230901"
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"display": "Epsilon gamma delta beta thalassemia (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
"code": "234383000",
"system": "http://snomed.info/sct",
"display": "Homozygous alpha thalassemia (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
"code": "234385007",
"system": "http://snomed.info/sct",
"display": "Alpha thalassemia-2 trait (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
"code": "234386008",
"system": "http://snomed.info/sct",
"display": "Hemoglobin Constant Spring trait (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
"code": "234387004",
"system": "http://snomed.info/sct",
"display": "Hemoglobin Lepore trait (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
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"system": "http://snomed.info/sct",
"display": "Delta-beta-Lepore thalassemia (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
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"system": "http://snomed.info/sct",
"display": "Alpha-beta thalassemia (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
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"version": "http://snomed.info/sct/731000124108/version/20230901"
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"display": "Homozygous beta thalassemia (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
"code": "269175006",
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"display": "Beta thalassemia trait (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
"code": "27080008",
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"display": "Beta zero thalassemia deletion type (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
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"version": "http://snomed.info/sct/731000124108/version/20230901"
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"display": "Hereditary persistence of fetal hemoglobin unlinked to beta-globulin gene cluster (disorder)",
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"version": "http://snomed.info/sct/731000124108/version/20230901"
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"system": "http://snomed.info/sct",
"display": "Sickle cell-thalassemia disease (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
"code": "39586009",
"system": "http://snomed.info/sct",
"display": "Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
"code": "40108008",
"system": "http://snomed.info/sct",
"display": "Thalassemia (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
"code": "416826005",
"system": "http://snomed.info/sct",
"display": "Sickle cell-thalassemia disease with crisis (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
"code": "417048006",
"system": "http://snomed.info/sct",
"display": "Sickle cell-thalassemia disease without crisis (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
"code": "447117006",
"system": "http://snomed.info/sct",
"display": "Hemoglobin H constant spring thalassemia (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
"code": "47047009",
"system": "http://snomed.info/sct",
"display": "Thalassemia with other hemoglobinopathy (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
"code": "47084006",
"system": "http://snomed.info/sct",
"display": "Beta plus thalassemia normal hemoglobin A>2< type 1 silent (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
"code": "48553001",
"system": "http://snomed.info/sct",
"display": "Hemoglobin H disease (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
"code": "5300004",
"system": "http://snomed.info/sct",
"display": "Hemoglobin Bart's hydrops syndrome (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
"code": "54006005",
"system": "http://snomed.info/sct",
"display": "Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
"code": "56205004",
"system": "http://snomed.info/sct",
"display": "Hereditary persistence of fetal hemoglobin, nondeletion type (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
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"code": "5967006",
"system": "http://snomed.info/sct",
"display": "A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis (disorder)",
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}, {
"code": "61395005",
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"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
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"system": "http://snomed.info/sct",
"display": "Thalassemia-hemoglobin C disease (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
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"system": "http://snomed.info/sct",
"display": "Delta zero thalassemia (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
}, {
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"version": "http://snomed.info/sct/731000124108/version/20230901"
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}, {
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"version": "http://snomed.info/sct/731000124108/version/20230901"
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"code": "89810003",
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"display": "^A^gamma delta beta^0^ thalassemia (disorder)",
"version": "http://snomed.info/sct/731000124108/version/20230901"
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} ],
"timestamp": "2023-12-11T00:15:34-05:00",
"identifier": "urn:uuid:63da816e-d9f7-45f7-8e02-12f706044a49"
},
"title": "Thalassemia",
"package_version": "0.17.0",
"extension": [ {
"url": "http://hl7.org/fhir/StructureDefinition/valueset-author",
"valueString": "MCC eCare Plan Author"
}, {
"url": "http://hl7.org/fhir/StructureDefinition/resource-lastReviewDate",
"valueDate": "2022-12-15"
}, {
"url": "http://hl7.org/fhir/StructureDefinition/valueset-effectiveDate",
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} ],
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"identifier": [ {
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"system": "urn:ietf:rfc:3986"
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}