Thalassemia
retiredURL
http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1222.772Copied!
Version20210916Copied!
PublisherHL7 Patient Care WG StewardDate2021-09-16T01:01:06-04:00Purpose(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.)
Expansion
Expansion error
Can't resolve code system: http://snomed.info/sct|http://snomed.info/sct/731000124108/version/20240301
systemhttp://snomed.info/sct
versionhttp://snomed.info/sct/731000124108/version/20240301
filterconceptis-a40108008
{
"compose" : {
"exclude" : [ ],
"include" : [ {
"system" : "http://snomed.info/sct",
"filter" : [ {
"property" : "concept",
"value" : "40108008",
"op" : "is-a"
} ],
"version" : "http://snomed.info/sct/731000124108/version/20240301"
} ]
},
"date" : "2021-09-16T01:01:06-04:00",
"meta" : {
"versionId" : "5",
"lastUpdated" : "2024-01-12T10:17:05.000-05:00",
"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" ]
},
"publisher" : "HL7 Patient Care WG Steward",
"jurisdiction" : [ {
"coding" : [ {
"system" : "urn:iso:std:iso:3166",
"code" : "US"
} ]
} ],
"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",
"experimental" : false,
"resourceType" : "ValueSet",
"expansion" : {
"contains" : [ {
"system" : "http://snomed.info/sct",
"code" : "10806241000119108",
"display" : "Thalassemia in mother complicating childbirth (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "111572002",
"display" : "Beta zero thalassemia non deletion type (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "1148897000",
"display" : "Hemoglobin Paksé disease (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "1148899002",
"display" : "Hemoglobin Seal Rock disease (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "119641000119103",
"display" : "Homozygous hemoglobin H constant spring thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "119691000119106",
"display" : "Hemoglobin C/beta thalassemia disease (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "119701000119106",
"display" : "Hemoglobin D/beta thalassemia disease (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "127041004",
"display" : "Sickle cell-beta-thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "127042006",
"display" : "Sickle cell beta plus thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "127043001",
"display" : "Sickle cell-beta^0^-thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "127044007",
"display" : "Sickle cell-delta beta^0^-thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "127045008",
"display" : "Sickle cell anemia with coexistent alpha-thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "127046009",
"display" : "Sickle cell trait with coexistent alpha-thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "15326009",
"display" : "beta^+^ Thalassemia, normal Hb A>2<, type 2 (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "16360009",
"display" : "Delta beta thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "16427007",
"display" : "Delta thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "16964007",
"display" : "Hereditary persistence of fetal hemoglobin thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "191187006",
"display" : "Alpha trait thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "191189009",
"display" : "Beta thalassemia intermedia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "19442009",
"display" : "Heterozygous thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "23371004",
"display" : "Epsilon gamma delta beta thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "234383000",
"display" : "Homozygous alpha thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "234385007",
"display" : "Alpha thalassemia-2 trait (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "234386008",
"display" : "Hemoglobin Constant Spring trait (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "234387004",
"display" : "Hemoglobin Lepore trait (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "234388009",
"display" : "Delta-beta-Lepore thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "234389001",
"display" : "Alpha-beta thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "234390005",
"display" : "Gamma thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "234392002",
"display" : "Hemoglobin E/beta thalassemia disease (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "26682008",
"display" : "Homozygous beta thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "269175006",
"display" : "Beta thalassemia trait (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "27080008",
"display" : "Beta zero thalassemia deletion type (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "307343001",
"display" : "Acquired hemoglobin H disease (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "32855007",
"display" : "Hereditary persistence of fetal hemoglobin unlinked to beta-globulin gene cluster (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "36467003",
"display" : "Alpha plus thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "36472007",
"display" : "Sickle cell-thalassemia disease (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "39586009",
"display" : "Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "40108008",
"display" : "Thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "416826005",
"display" : "Sickle cell-thalassemia disease with crisis (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "417048006",
"display" : "Sickle cell-thalassemia disease without crisis (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "447117006",
"display" : "Hemoglobin H constant spring thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "47047009",
"display" : "Thalassemia with other hemoglobinopathy (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "47084006",
"display" : "Beta plus thalassemia normal hemoglobin A>2< type 1 silent (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "48553001",
"display" : "Hemoglobin H disease (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "5300004",
"display" : "Hemoglobin Bart's hydrops syndrome (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "54006005",
"display" : "Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "56205004",
"display" : "Hereditary persistence of fetal hemoglobin, nondeletion type (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "5967006",
"display" : "A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "61395005",
"display" : "Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "61777009",
"display" : "Thalassemia-hemoglobin C disease (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "62074008",
"display" : "Delta zero thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "65959000",
"display" : "Beta thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "66055002",
"display" : "Alpha zero thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "685061000119108",
"display" : "Hemoglobin C beta plus thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "685071000119102",
"display" : "Hemoglobin C beta zero thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "685081000119104",
"display" : "Hemoglobin D beta plus thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "685091000119101",
"display" : "Hemoglobin D beta zero thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "685101000119106",
"display" : "Hemoglobin E beta plus thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "685111000119109",
"display" : "Hemoglobin E beta zero thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "68913001",
"display" : "Alpha thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "69216008",
"display" : "Hb Lepore thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "715342005",
"display" : "Alpha thalassemia X-linked intellectual disability syndrome (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "716682000",
"display" : "Dominant beta-thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "718196002",
"display" : "Beta thalassemia X-linked thrombocytopenia syndrome (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "72331000119105",
"display" : "Thalassemia in mother complicating pregnancy (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "73190000",
"display" : "Epsilon gamma delta beta^0^ thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "734349003",
"display" : "Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "75451007",
"display" : "Thalassemia major (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "76336008",
"display" : "Delta beta zero thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "788944005",
"display" : "Gamma delta beta thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "79592006",
"display" : "Beta plus thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "84188003",
"display" : "Thalassemia syndrome (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "85422000",
"display" : "Alpha plus thalassemia non deletion type (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "85557000",
"display" : "Hereditary persistence of fetal hemoglobin deletion type (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "86242003",
"display" : "Alpha plus thalassemia deletion type (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "86715000",
"display" : "Beta zero thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "89459006",
"display" : "Hereditary persistence of fetal hemoglobin linked to beta-globulin gene cluster (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "89810003",
"display" : "^A^gamma delta beta^0^ thalassemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
}, {
"system" : "http://snomed.info/sct",
"code" : "934007",
"display" : "Thalassemia intermedia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20240301"
} ],
"total" : 79,
"identifier" : "urn:uuid:9d7f8709-0906-41f3-9bc1-c1c09c59de73",
"timestamp" : "2024-06-14T14:29:51-04:00"
},
"title" : "Thalassemia",
"extension" : [ {
"valueString" : "MCC eCare Plan Author",
"url" : "http://hl7.org/fhir/StructureDefinition/valueset-author"
}, {
"valueString" : "MCC_IG",
"url" : "http://hl7.org/fhir/StructureDefinition/valueset-keyWord"
}, {
"valueDate" : "2024-06-03",
"url" : "http://hl7.org/fhir/StructureDefinition/resource-lastReviewDate"
}, {
"valueDate" : "2021-09-16",
"url" : "http://hl7.org/fhir/StructureDefinition/valueset-effectiveDate"
}, {
"url" : "http://health-samurai.io/extensions/source",
"valueCode" : "db"
} ],
"status" : "retired",
"id" : "2.16.840.1.113762.1.4.1222.772",
"url" : "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1222.772",
"identifier" : [ {
"system" : "urn:ietf:rfc:3986",
"value" : "urn:oid:2.16.840.1.113762.1.4.1222.772"
} ],
"version" : "20210916"
}