Immunodeficient Conditions SM CT
activeURL
http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.666.5.2342Copied!
Version20160331Copied!
PublisherLantana EH StewardDate2016-03-31T01:00:12-04:00Purpose(Clinical Focus: This set of values contains diagnoses most commonly used for patients with Immunodeficiency conditions.),(Data Element Scope: The intent of this data element is to identify patients who have an active diagnosis of an immunodeficiency conditions. Using the Quality Data Model, this particular element will map to the Diagnosis category.),(Inclusion Criteria: Include codes representing a diagnosis of immunodeficient conditions including acquired immune deficiency syndrome, AIDS related Complex, Immunodeficiency Syndromes, Chronic Lymphocytic Leukemia, congenital or hereditary immunodeficiency, human immunodeficiency virus, HIV positive and organ transplant using the SNOMED CT code system.),(Exclusion Criteria: None.)
Expansion
| Code | Display | System |
|---|---|---|
| 3439009 | http://snomed.info/sct | |
| 5810003 | http://snomed.info/sct | |
| 9893005 | http://snomed.info/sct | |
| 21527007 | http://snomed.info/sct | |
| 22406001 | http://snomed.info/sct | |
| 23238000 | http://snomed.info/sct | |
| 25109007 | http://snomed.info/sct | |
| 26252007 | http://snomed.info/sct | |
| 29272001 | http://snomed.info/sct | |
| 31323000 | http://snomed.info/sct | |
| 33286000 | http://snomed.info/sct | |
| 36070007 | http://snomed.info/sct | |
| 36138009 | http://snomed.info/sct | |
| 36980009 | http://snomed.info/sct | |
| 37548006 | http://snomed.info/sct | |
| 40197009 | http://snomed.info/sct | |
| 40780007 | http://snomed.info/sct | |
| 45390000 | http://snomed.info/sct | |
| 48794007 | http://snomed.info/sct | |
| 49555001 | http://snomed.info/sct |
systemhttp://snomed.info/sct
{
"compose" : {
"exclude" : [ ],
"include" : [ {
"system" : "http://snomed.info/sct",
"extension" : [ {
"extension" : [ {
"valueString" : "concept",
"url" : "path"
}, {
"url" : "count",
"valueInteger" : 124
} ],
"url" : "http://health-samurai.io/extensions/excised-data"
} ]
} ]
},
"date" : "2016-03-31T01:00:12-04:00",
"meta" : {
"versionId" : "22",
"lastUpdated" : "2023-12-21T17:43:03.000-05:00",
"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" : "Lantana EH Steward",
"jurisdiction" : [ {
"coding" : [ {
"system" : "urn:iso:std:iso:3166",
"code" : "US"
} ]
} ],
"purpose" : "(Clinical Focus: This set of values contains diagnoses most commonly used for patients with Immunodeficiency conditions.),(Data Element Scope: The intent of this data element is to identify patients who have an active diagnosis of an immunodeficiency conditions. Using the Quality Data Model, this particular element will map to the Diagnosis category.),(Inclusion Criteria: Include codes representing a diagnosis of immunodeficient conditions including acquired immune deficiency syndrome, AIDS related Complex, Immunodeficiency Syndromes, Chronic Lymphocytic Leukemia, congenital or hereditary immunodeficiency, human immunodeficiency virus, HIV positive and organ transplant using the SNOMED CT code system.),(Exclusion Criteria: None.)",
"name" : "ImmunodeficientConditionsSMCT",
"experimental" : false,
"resourceType" : "ValueSet",
"expansion" : {
"contains" : [ {
"system" : "http://snomed.info/sct",
"code" : "103077004",
"display" : "Immunodeficiency secondary to neoplasm (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "103078009",
"display" : "Immunodeficiency secondary to trauma (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "103079001",
"display" : "Immunodeficiency caused by corticosteroid (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "103080003",
"display" : "Immunodeficiency secondary to radiation therapy (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "103081004",
"display" : "Immunodeficiency secondary to chemotherapy (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "111584000",
"display" : "Reticular dysgenesis (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "111587007",
"display" : "Severe combined immunodeficiency due to absent interleukin-2 receptor (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "111880001",
"display" : "Acute human immunodeficiency virus infection (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "186706006",
"display" : "Human immunodeficiency virus infection constitutional disease (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "186707002",
"display" : "Human immunodeficiency virus infection with neurological disease (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "186708007",
"display" : "Human immunodeficiency virus infection with secondary clinical infectious disease (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "190979003",
"display" : "Selective immunoglobulin A deficiency (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "190980000",
"display" : "Selective immunoglobulin M deficiency (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "190981001",
"display" : "Selective immunoglobulin G deficiency (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "190995003",
"display" : "Thymic aplasia or dysplasia with immunodeficiency (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "190997006",
"display" : "Severe combined immunodeficiency with low T- and B-cell numbers (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "190998001",
"display" : "Severe combined immunodeficiency with low or normal B-cell numbers (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "191008001",
"display" : "Immunodeficiency following hereditary defective response to Epstein-Barr virus (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "191011000",
"display" : "Common variable immunodeficiency with predominant abnormalities of B-cell numbers and functions (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "191012007",
"display" : "Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "191013002",
"display" : "Common variable immunodeficiency with autoantibodies to B- or T-cells (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "21527007",
"display" : "Chronic granulomatous disease, type IV (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "22406001",
"display" : "Severe combined immunodeficiency due to absent lymphoid stem cells (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "230180003",
"display" : "Human immunodeficiency virus leukoencephalopathy (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "23238000",
"display" : "Common variable agammaglobulinemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "234532001",
"display" : "Immunodeficiency disorder (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "234533006",
"display" : "X-linked agammaglobulinemia with growth hormone deficiency (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "234570002",
"display" : "Severe combined immunodeficiency with maternofetal engraftment (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "234572005",
"display" : "Benign combined immunodeficiency (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "234631003",
"display" : "Immunodeficiency with major anomalies (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "234632005",
"display" : "Immunodeficiency associated with chromosomal abnormality (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "234633000",
"display" : "Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "234638009",
"display" : "Microcephaly, normal intelligence and immunodeficiency (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "234641000",
"display" : "Immunodeficiency associated with multiple organ system abnormalities (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "234642007",
"display" : "Age-related immunodeficiency (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "234645009",
"display" : "Drug-induced immunodeficiency (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "234997004",
"display" : "Chronic gingival granulomatous condition (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "235662006",
"display" : "Chronic granulomatous gastritis (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "235726002",
"display" : "Human immunodeficiency virus enteropathy (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "236406007",
"display" : "Acquired immune deficiency syndrome-related nephropathy (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "240103002",
"display" : "Human immunodeficiency virus myopathy (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "26252007",
"display" : "Chronic granulomatous disease, type IIA (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "276665006",
"display" : "Congenital acquired immune deficiency syndrome (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "276666007",
"display" : "Congenital human immunodeficiency virus positive status syndrome (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "277549009",
"display" : "Chronic lymphocytic prolymphocytic leukemia syndrome (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "281388009",
"display" : "Human immunodeficiency virus-related sclerosing cholangitis (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "29272001",
"display" : "Chronic granulomatous disease, type I (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "31323000",
"display" : "Severe combined immunodeficiency disease (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "315019000",
"display" : "Human immunodeficiency virus infection with aseptic meningitis (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "33286000",
"display" : "Secondary immune deficiency disorder (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "3439009",
"display" : "Severe combined immunodeficiency due to absent peripheral T cell maturation (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "350353007",
"display" : "De Vaal's syndrome (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "36070007",
"display" : "Wiskott-Aldrich syndrome (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "36138009",
"display" : "Congenital immunodeficiency disease (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "362993009",
"display" : "Autosomal recessive severe combined immunodeficiency disease (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "363040003",
"display" : "Congenital immunodeficiency involving the hematopoietic system (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "36980009",
"display" : "Severe combined immunodeficiency due to absent adenosine deaminase (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "37548006",
"display" : "Hypopigmentation-immunodeficiency disease (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "387759001",
"display" : "Chronic granulomatous disease (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "398329009",
"display" : "Human immunodeficiency virus encephalitis (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "40197009",
"display" : "Chronic granulomatous disease, type IA (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "402791005",
"display" : "B-lymphocyte immunodeficiency (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "402792003",
"display" : "T-lymphocyte immunodeficiency (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "402900005",
"display" : "Oral hairy leukoplakia associated with immunodeficiency (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "402901009",
"display" : "Oral hairy leukoplakia associated with human immunodeficiency virus disease (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "403835002",
"display" : "X-linked hyper-immunoglobulin M syndrome (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "40780007",
"display" : "Human immunodeficiency virus I infection (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "414376003",
"display" : "Hairy leukoplakia of tongue associated with human immunodeficiency virus disease (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "414604009",
"display" : "Leukoplakia of tongue associated with human immunodeficiency virus disease (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "421047005",
"display" : "Candidiasis of lung with acquired immunodeficiency syndrome (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "430338009",
"display" : "Smoldering chronic lymphocytic leukemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "442134007",
"display" : "Hepatitis B associated with Human immunodeficiency virus infection (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "442459007",
"display" : "Combined immunodeficiency disease (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "442537007",
"display" : "Non-Hodgkin lymphoma associated with Human immunodeficiency virus infection (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "445945000",
"display" : "Infectious disease with acquired immune deficiency syndrome (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "45390000",
"display" : "Severe combined immunodeficiency due to absent interleukin-2 production (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "48794007",
"display" : "Human immunodeficiency virus infection with infectious mononucleosis-like syndrome (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "49555001",
"display" : "Severe combined immunodeficiency due to absent T cell receptor (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "52079000",
"display" : "Congenital human immunodeficiency virus infection (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "58606001",
"display" : "Primary immune deficiency disorder (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "62479008",
"display" : "Acquired immune deficiency syndrome (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "65880007",
"display" : "X-linked agammaglobulinemia (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "71904008",
"display" : "Severe combined immunodeficiency due to absent class II human leukocyte antigens (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "71943007",
"display" : "Chronic granulomatous tuberculosis (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "76243000",
"display" : "Chronic granulomatous disease, type IVA (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "77330006",
"display" : "Chronic granulomatous disease, type II (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "79019005",
"display" : "Human immunodeficiency virus II infection (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "81000119104",
"display" : "Symptomatic human immunodeficiency virus infection (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "82286005",
"display" : "Hyperimmunoglobulin M syndrome (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "82317007",
"display" : "Chronic granulomatous disease, type III (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "86406008",
"display" : "Human immunodeficiency virus infection (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "87117006",
"display" : "Human immunodeficiency virus infection with acute lymphadenitis (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "91947003",
"display" : "Asymptomatic human immunodeficiency virus infection (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "91948008",
"display" : "Asymptomatic human immunodeficiency virus infection in pregnancy (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "92814006",
"display" : "Chronic lymphoid leukemia, disease (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "95892003",
"display" : "Persistent generalized lymphadenopathy (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
}, {
"system" : "http://snomed.info/sct",
"code" : "9893005",
"display" : "Immunodeficiency with thymoma (disorder)",
"version" : "http://snomed.info/sct/731000124108/version/20230901"
} ],
"total" : 97,
"identifier" : "urn:uuid:9936564e-249a-4316-bfd1-6b8290c1be74",
"timestamp" : "2024-04-23T19:50:19-04:00"
},
"title" : "Immunodeficient Conditions SM CT",
"extension" : [ {
"valueString" : "Lantana EH Author",
"url" : "http://hl7.org/fhir/StructureDefinition/valueset-author"
}, {
"valueDate" : "2022-12-15",
"url" : "http://hl7.org/fhir/StructureDefinition/resource-lastReviewDate"
}, {
"valueDate" : "2016-03-31",
"url" : "http://hl7.org/fhir/StructureDefinition/valueset-effectiveDate"
}, {
"url" : "http://health-samurai.io/extensions/source",
"valueCode" : "db"
} ],
"status" : "active",
"id" : "5c71ce8d-8380-49f0-8408-5a96c406ef73",
"url" : "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.666.5.2342",
"identifier" : [ {
"system" : "urn:ietf:rfc:3986",
"value" : "urn:oid:2.16.840.1.113883.3.666.5.2342"
} ],
"version" : "20160331"
}