| Source | us.nlm.vsac#0.11.0:null (v4.0.1) |
| resourceType | ValueSet |
| id | 2.16.840.1.113883.3.666.5.2342 |
| canonical | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.666.5.2342 |
| version | 20160331 |
| status | active |
| publisher | Lantana EH Steward |
| name | ImmunodeficientConditionsSMCT |
| title | Immunodeficient Conditions SM CT |
| date | 2016-03-31T01:00:12-04:00 |
| experimental | false |
| Usages |
|
This value set contains 97 concepts
| Code | System | Display |
| 103077004 | http://snomed.info/sct | Immunodeficiency secondary to neoplasm (disorder) |
| 103078009 | http://snomed.info/sct | Immunodeficiency secondary to trauma (disorder) |
| 103079001 | http://snomed.info/sct | Immunodeficiency caused by corticosteroid (disorder) |
| 103080003 | http://snomed.info/sct | Immunodeficiency secondary to radiation therapy (disorder) |
| 103081004 | http://snomed.info/sct | Immunodeficiency secondary to chemotherapy (disorder) |
| 111584000 | http://snomed.info/sct | Reticular dysgenesis (disorder) |
| 111587007 | http://snomed.info/sct | Severe combined immunodeficiency due to absent interleukin-2 receptor (disorder) |
| 111880001 | http://snomed.info/sct | Acute human immunodeficiency virus infection (disorder) |
| 186706006 | http://snomed.info/sct | Human immunodeficiency virus infection constitutional disease (disorder) |
| 186707002 | http://snomed.info/sct | Human immunodeficiency virus infection with neurological disease (disorder) |
| 186708007 | http://snomed.info/sct | Human immunodeficiency virus infection with secondary clinical infectious disease (disorder) |
| 190979003 | http://snomed.info/sct | Selective immunoglobulin A deficiency (disorder) |
| 190980000 | http://snomed.info/sct | Selective immunoglobulin M deficiency (disorder) |
| 190981001 | http://snomed.info/sct | Selective immunoglobulin G deficiency (disorder) |
| 190995003 | http://snomed.info/sct | Thymic aplasia or dysplasia with immunodeficiency (disorder) |
| 190997006 | http://snomed.info/sct | Severe combined immunodeficiency with low T- and B-cell numbers (disorder) |
| 190998001 | http://snomed.info/sct | Severe combined immunodeficiency with low or normal B-cell numbers (disorder) |
| 191008001 | http://snomed.info/sct | Immunodeficiency following hereditary defective response to Epstein-Barr virus (disorder) |
| 191011000 | http://snomed.info/sct | Common variable immunodeficiency with predominant abnormalities of B-cell numbers and functions (disorder) |
| 191012007 | http://snomed.info/sct | Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder) |
| 191013002 | http://snomed.info/sct | Common variable immunodeficiency with autoantibodies to B- or T-cells (disorder) |
| 21527007 | http://snomed.info/sct | Chronic granulomatous disease, type IV (disorder) |
| 22406001 | http://snomed.info/sct | Severe combined immunodeficiency due to absent lymphoid stem cells (disorder) |
| 230180003 | http://snomed.info/sct | Human immunodeficiency virus leukoencephalopathy (disorder) |
| 23238000 | http://snomed.info/sct | Common variable agammaglobulinemia (disorder) |
| 234532001 | http://snomed.info/sct | Immunodeficiency disorder (disorder) |
| 234533006 | http://snomed.info/sct | X-linked agammaglobulinemia with growth hormone deficiency (disorder) |
| 234570002 | http://snomed.info/sct | Severe combined immunodeficiency with maternofetal engraftment (disorder) |
| 234572005 | http://snomed.info/sct | Benign combined immunodeficiency (disorder) |
| 234631003 | http://snomed.info/sct | Immunodeficiency with major anomalies (disorder) |
| 234632005 | http://snomed.info/sct | Immunodeficiency associated with chromosomal abnormality (disorder) |
| 234633000 | http://snomed.info/sct | Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency (disorder) |
| 234638009 | http://snomed.info/sct | Microcephaly, normal intelligence and immunodeficiency (disorder) |
| 234641000 | http://snomed.info/sct | Immunodeficiency associated with multiple organ system abnormalities (disorder) |
| 234642007 | http://snomed.info/sct | Age-related immunodeficiency (disorder) |
| 234645009 | http://snomed.info/sct | Drug-induced immunodeficiency (disorder) |
| 234997004 | http://snomed.info/sct | Chronic gingival granulomatous condition (disorder) |
| 235662006 | http://snomed.info/sct | Chronic granulomatous gastritis (disorder) |
| 235726002 | http://snomed.info/sct | Human immunodeficiency virus enteropathy (disorder) |
| 236406007 | http://snomed.info/sct | Acquired immune deficiency syndrome-related nephropathy (disorder) |
| 240103002 | http://snomed.info/sct | Human immunodeficiency virus myopathy (disorder) |
| 26252007 | http://snomed.info/sct | Chronic granulomatous disease, type IIA (disorder) |
| 276665006 | http://snomed.info/sct | Congenital acquired immune deficiency syndrome (disorder) |
| 276666007 | http://snomed.info/sct | Congenital human immunodeficiency virus positive status syndrome (disorder) |
| 277549009 | http://snomed.info/sct | Chronic lymphocytic prolymphocytic leukemia syndrome (disorder) |
| 281388009 | http://snomed.info/sct | Human immunodeficiency virus-related sclerosing cholangitis (disorder) |
| 29272001 | http://snomed.info/sct | Chronic granulomatous disease, type I (disorder) |
| 31323000 | http://snomed.info/sct | Severe combined immunodeficiency disease (disorder) |
| 315019000 | http://snomed.info/sct | Human immunodeficiency virus infection with aseptic meningitis (disorder) |
| 33286000 | http://snomed.info/sct | Secondary immune deficiency disorder (disorder) |
| 3439009 | http://snomed.info/sct | Severe combined immunodeficiency due to absent peripheral T cell maturation (disorder) |
| 350353007 | http://snomed.info/sct | De Vaal's syndrome (disorder) |
| 36070007 | http://snomed.info/sct | Wiskott-Aldrich syndrome (disorder) |
| 36138009 | http://snomed.info/sct | Congenital immunodeficiency disease (disorder) |
| 362993009 | http://snomed.info/sct | Autosomal recessive severe combined immunodeficiency disease (disorder) |
| 363040003 | http://snomed.info/sct | Congenital immunodeficiency involving the hematopoietic system (disorder) |
| 36980009 | http://snomed.info/sct | Severe combined immunodeficiency due to absent adenosine deaminase (disorder) |
| 37548006 | http://snomed.info/sct | Hypopigmentation-immunodeficiency disease (disorder) |
| 387759001 | http://snomed.info/sct | Chronic granulomatous disease (disorder) |
| 398329009 | http://snomed.info/sct | Human immunodeficiency virus encephalitis (disorder) |
| 40197009 | http://snomed.info/sct | Chronic granulomatous disease, type IA (disorder) |
| 402791005 | http://snomed.info/sct | B-lymphocyte immunodeficiency (disorder) |
| 402792003 | http://snomed.info/sct | T-lymphocyte immunodeficiency (disorder) |
| 402900005 | http://snomed.info/sct | Oral hairy leukoplakia associated with immunodeficiency (disorder) |
| 402901009 | http://snomed.info/sct | Oral hairy leukoplakia associated with human immunodeficiency virus disease (disorder) |
| 403835002 | http://snomed.info/sct | X-linked hyper-immunoglobulin M syndrome (disorder) |
| 40780007 | http://snomed.info/sct | Human immunodeficiency virus I infection (disorder) |
| 414376003 | http://snomed.info/sct | Hairy leukoplakia of tongue associated with human immunodeficiency virus disease (disorder) |
| 414604009 | http://snomed.info/sct | Leukoplakia of tongue associated with human immunodeficiency virus disease (disorder) |
| 421047005 | http://snomed.info/sct | Candidiasis of lung with acquired immunodeficiency syndrome (disorder) |
| 430338009 | http://snomed.info/sct | Smoldering chronic lymphocytic leukemia (disorder) |
| 442134007 | http://snomed.info/sct | Hepatitis B associated with Human immunodeficiency virus infection (disorder) |
| 442459007 | http://snomed.info/sct | Combined immunodeficiency disease (disorder) |
| 442537007 | http://snomed.info/sct | Non-Hodgkin lymphoma associated with Human immunodeficiency virus infection (disorder) |
| 445945000 | http://snomed.info/sct | Infectious disease with acquired immune deficiency syndrome (disorder) |
| 45390000 | http://snomed.info/sct | Severe combined immunodeficiency due to absent interleukin-2 production (disorder) |
| 48794007 | http://snomed.info/sct | Human immunodeficiency virus infection with infectious mononucleosis-like syndrome (disorder) |
| 49555001 | http://snomed.info/sct | Severe combined immunodeficiency due to absent T cell receptor (disorder) |
| 52079000 | http://snomed.info/sct | Congenital human immunodeficiency virus infection (disorder) |
| 58606001 | http://snomed.info/sct | Primary immune deficiency disorder (disorder) |
| 62479008 | http://snomed.info/sct | Acquired immune deficiency syndrome (disorder) |
| 65880007 | http://snomed.info/sct | X-linked agammaglobulinemia (disorder) |
| 71904008 | http://snomed.info/sct | Severe combined immunodeficiency due to absent class II human leukocyte antigens (disorder) |
| 71943007 | http://snomed.info/sct | Chronic granulomatous tuberculosis (disorder) |
| 76243000 | http://snomed.info/sct | Chronic granulomatous disease, type IVA (disorder) |
| 77330006 | http://snomed.info/sct | Chronic granulomatous disease, type II (disorder) |
| 79019005 | http://snomed.info/sct | Human immunodeficiency virus II infection (disorder) |
| 81000119104 | http://snomed.info/sct | Symptomatic human immunodeficiency virus infection (disorder) |
| 82286005 | http://snomed.info/sct | Hyperimmunoglobulin M syndrome (disorder) |
| 82317007 | http://snomed.info/sct | Chronic granulomatous disease, type III (disorder) |
| 86406008 | http://snomed.info/sct | Human immunodeficiency virus infection (disorder) |
| 87117006 | http://snomed.info/sct | Human immunodeficiency virus infection with acute lymphadenitis (disorder) |
| 91947003 | http://snomed.info/sct | Asymptomatic human immunodeficiency virus infection (disorder) |
| 91948008 | http://snomed.info/sct | Asymptomatic human immunodeficiency virus infection in pregnancy (disorder) |
| 92814006 | http://snomed.info/sct | Chronic lymphoid leukemia, disease (disorder) |
| 95892003 | http://snomed.info/sct | Persistent generalized lymphadenopathy (disorder) |
| 9893005 | http://snomed.info/sct | Immunodeficiency with thymoma (disorder) |
Produced 08 Sep 2023