| Source | us.nlm.vsac#0.11.0:null (v4.0.1) |
| resourceType | ValueSet |
| id | 2.16.840.1.113883.3.3616.200.110.102.6153 |
| canonical | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.3616.200.110.102.6153 |
| version | 20221210 |
| status | active |
| publisher | Clinical Architecture |
| name | COVID19SNOMEDValueSetForImmuneSystemDisorders |
| title | COVID19 SNOMED Value Set for Immune System Disorders |
| date | 2023-06-21T18:16:37-04:00 |
| Usages |
|
This value set contains 188 concepts
| Code | System | Display |
| 111584000 | http://snomed.info/sct | Reticular dysgenesis (disorder) |
| 111587007 | http://snomed.info/sct | Severe combined immunodeficiency due to absent interleukin-2 receptor (disorder) |
| 1144907001 | http://snomed.info/sct | Late acute graft-versus-host disease (disorder) |
| 1144908006 | http://snomed.info/sct | Late chronic graft-versus-host disease (disorder) |
| 1144963000 | http://snomed.info/sct | Acute on chronic graft-versus-host disease (disorder) |
| 1162263002 | http://snomed.info/sct | Complement component 8 deficiency (disorder) |
| 1177120001 | http://snomed.info/sct | Bronchiolitis obliterans syndrome due to and following allogeneic stem cell transplant (disorder) |
| 1177173001 | http://snomed.info/sct | Congenital progressive bone marrow failure, B-cell immunodeficiency, skeletal dysplasia syndrome (disorder) |
| 1177175008 | http://snomed.info/sct | Skeletal dysplasia, T-cell immunodeficiency, developmental delay syndrome (disorder) |
| 1179284005 | http://snomed.info/sct | Severe combined immunodeficiency due to linker for activation of T cells deficiency (disorder) |
| 1179285006 | http://snomed.info/sct | Combined immunodeficiency due to moesin deficiency (disorder) |
| 1179286007 | http://snomed.info/sct | Combined immunodeficiency due to GINS complex subunit 1 deficiency (disorder) |
| 1179288008 | http://snomed.info/sct | Combined immunodeficiency due to transferrin receptor deficiency (disorder) |
| 1179300002 | http://snomed.info/sct | B-cell expansion with nuclear factor kappa light chain enhancer of activated B cells and T-cell anergy disease (disorder) |
| 1186712009 | http://snomed.info/sct | Combined immunodeficiency due to capping protein regulator and myosin 1 linker 2 deficiency (disorder) |
| 1186714005 | http://snomed.info/sct | Combined immunodeficiency due to interleukin-2 inducible T cell kinase deficiency (disorder) |
| 1186715006 | http://snomed.info/sct | Combined immunodeficiency due to CD70 deficiency (disorder) |
| 1187623009 | http://snomed.info/sct | Phosphoglucomutase 3-related congenital disorder of glycosylation (disorder) |
| 1197205005 | http://snomed.info/sct | Combined immunodeficiency due to dedicator of cytokinesis 8 deficiency (disorder) |
| 1197428008 | http://snomed.info/sct | Combined immunodeficiency, enteropathy spectrum (disorder) |
| 1197477000 | http://snomed.info/sct | Combined immunodeficiency due to lipopolysaccharide-responsive beige-like anchor protein deficiency (disorder) |
| 1197478005 | http://snomed.info/sct | Primary immunodeficiency with multifaceted aberrant lymphoid immunity (disorder) |
| 1197479002 | http://snomed.info/sct | Dedicator of cytokinesis 2 deficiency (disorder) |
| 121121000119106 | http://snomed.info/sct | Acute graft-versus-host reaction following bone marrow transplant (disorder) |
| 1222681008 | http://snomed.info/sct | Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome (disorder) |
| 1229940001 | http://snomed.info/sct | Autosomal recessive T-cell negative, B-cell positive severe combined immunodeficiency due to interleukin 7 receptor deficiency (disorder) |
| 1229941002 | http://snomed.info/sct | Autosomal recessive T-cell negative, B-cell positive severe combined immunodeficiency due to protein tyrosine phosphatase receptor type C deficiency (disorder) |
| 1229942009 | http://snomed.info/sct | Severe combined immunodeficiency due to coronin 1A deficiency (disorder) |
| 1230015008 | http://snomed.info/sct | Hereditary angioedema with C1 esterase inhibitor deficiency (disorder) |
| 128631000119109 | http://snomed.info/sct | Chronic graft-versus-host disease following kidney transplant (disorder) |
| 18827005 | http://snomed.info/sct | Complement abnormality (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) |
| 190996002 | http://snomed.info/sct | Severe combined immunodeficiency with reticular dysgenesis (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) |
| 191001007 | http://snomed.info/sct | Major histocompatibility complex class I deficiency (disorder) |
| 191002000 | http://snomed.info/sct | Major histocompatibility complex class II deficiency (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) |
| 191018006 | http://snomed.info/sct | Lymphocyte function antigen-1 defect (disorder) |
| 22406001 | http://snomed.info/sct | Severe combined immunodeficiency due to absent lymphoid stem cells (disorder) |
| 23238000 | http://snomed.info/sct | Common variable agammaglobulinemia (disorder) |
| 234146006 | http://snomed.info/sct | Hennekam lymphangiectasia-lymphedema syndrome (disorder) |
| 234532001 | http://snomed.info/sct | Immunodeficiency disorder (disorder) |
| 234539005 | http://snomed.info/sct | Immunoglobulin heavy chain deficiency (disorder) |
| 234540007 | http://snomed.info/sct | Selective immunoglobulin E deficiency (disorder) |
| 234541006 | http://snomed.info/sct | Selective immunoglobulin D deficiency (disorder) |
| 234542004 | http://snomed.info/sct | Selective immunoglobulin M and immunoglobulin A deficiency (disorder) |
| 234543009 | http://snomed.info/sct | Immunoglobulin light chain deficiency (disorder) |
| 234562007 | http://snomed.info/sct | Anti-protein antibody deficiency (disorder) |
| 234570002 | http://snomed.info/sct | Severe combined immunodeficiency with maternofetal engraftment (disorder) |
| 234571003 | http://snomed.info/sct | Warts, hypogammaglobulinemia, infections, and myelokathexis (disorder) |
| 234572005 | http://snomed.info/sct | Benign combined immunodeficiency (disorder) |
| 234593008 | http://snomed.info/sct | Classical complement pathway abnormality (disorder) |
| 234594002 | http://snomed.info/sct | Complement 1q deficiency (disorder) |
| 234595001 | http://snomed.info/sct | Complement 1q beta chain deficiency (disorder) |
| 234596000 | http://snomed.info/sct | Complement 1q dysfunction (disorder) |
| 234597009 | http://snomed.info/sct | Complement 1r deficiency (disorder) |
| 234598004 | http://snomed.info/sct | Complement 1s deficiency (disorder) |
| 234599007 | http://snomed.info/sct | Complement 2 deficiency (disorder) |
| 234600005 | http://snomed.info/sct | Complement 4 deficiency (disorder) |
| 234601009 | http://snomed.info/sct | Complement 4A deficiency (disorder) |
| 234602002 | http://snomed.info/sct | Complement 4B deficiency (disorder) |
| 234604001 | http://snomed.info/sct | Alternative pathway deficiency (disorder) |
| 234605000 | http://snomed.info/sct | Factor B deficiency (disorder) |
| 234607008 | http://snomed.info/sct | Factor D deficiency (disorder) |
| 234608003 | http://snomed.info/sct | Terminal component deficiency (disorder) |
| 234609006 | http://snomed.info/sct | Complement 5 deficiency (disorder) |
| 234611002 | http://snomed.info/sct | Complement 6 deficiency (disorder) |
| 234612009 | http://snomed.info/sct | Complement 7 deficiency (disorder) |
| 234613004 | http://snomed.info/sct | Combined complement 6 and 7 deficiencies (disorder) |
| 234614005 | http://snomed.info/sct | Complement 8 beta chain deficiency (disorder) |
| 234615006 | http://snomed.info/sct | Complement 8 beta chain dysfunction (disorder) |
| 234616007 | http://snomed.info/sct | Complement 8 alpha-gamma deficiency (disorder) |
| 234617003 | http://snomed.info/sct | Complement 9 deficiency (disorder) |
| 234618008 | http://snomed.info/sct | Complement regulatory factor defect (disorder) |
| 234619000 | http://snomed.info/sct | Hereditary C1 esterase inhibitor deficiency - deficient factor (disorder) |
| 234620006 | http://snomed.info/sct | Hereditary C1 esterase inhibitor deficiency - dysfunctional factor (disorder) |
| 234621005 | http://snomed.info/sct | Factor I deficiency (disorder) |
| 234622003 | http://snomed.info/sct | Factor H deficiency (disorder) |
| 234623008 | http://snomed.info/sct | Complement 4 binding protein deficiency (disorder) |
| 234624002 | http://snomed.info/sct | Decay accelerating factor deficiency (disorder) |
| 234625001 | http://snomed.info/sct | Homologous restriction factor deficiency (disorder) |
| 234626000 | http://snomed.info/sct | Complement 5a inhibitor deficiency (disorder) |
| 234627009 | http://snomed.info/sct | Anaphylotoxin inactivator deficiency (disorder) |
| 234628004 | http://snomed.info/sct | Complement receptor deficiency (disorder) |
| 234629007 | http://snomed.info/sct | Complement receptor 1 deficiency (disorder) |
| 234630002 | http://snomed.info/sct | Complement receptor 3 deficiency (disorder) |
| 234631003 | http://snomed.info/sct | Immunodeficiency with major anomalies (disorder) |
| 234641000 | http://snomed.info/sct | Immunodeficiency associated with multiple organ system abnormalities (disorder) |
| 234646005 | http://snomed.info/sct | Graft-versus-host disease (disorder) |
| 24419001 | http://snomed.info/sct | Disorder of complement (disorder) |
| 24743004 | http://snomed.info/sct | Complement deficiency disease (disorder) |
| 254067002 | http://snomed.info/sct | Immuno-osseous dysplasia (disorder) |
| 263661007 | http://snomed.info/sct | Complement 5 dysfunction (disorder) |
| 31323000 | http://snomed.info/sct | Severe combined immunodeficiency disease (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) |
| 351287008 | http://snomed.info/sct | Reticular dysgenesis with congenital aleukocytosis (disorder) |
| 36070007 | http://snomed.info/sct | Wiskott-Aldrich syndrome (disorder) |
| 362993009 | http://snomed.info/sct | Autosomal recessive severe combined immunodeficiency disease (disorder) |
| 36980009 | http://snomed.info/sct | Severe combined immunodeficiency due to absent adenosine deaminase (disorder) |
| 37548006 | http://snomed.info/sct | Hypopigmentation-immunodeficiency disease (disorder) |
| 39674000 | http://snomed.info/sct | Familial C3B inhibitor deficiency syndrome (disorder) |
| 402355000 | http://snomed.info/sct | Acute graft-versus-host disease (disorder) |
| 402356004 | http://snomed.info/sct | Chronic graft-versus-host disease (disorder) |
| 402357008 | http://snomed.info/sct | Lichenoid chronic graft-versus-host disease (disorder) |
| 402358003 | http://snomed.info/sct | Sclerodermoid chronic graft-versus-host disease (disorder) |
| 402360001 | http://snomed.info/sct | Materno-fetal graft-versus-host disease (disorder) |
| 403835002 | http://snomed.info/sct | X-linked hyper-immunoglobulin M syndrome (disorder) |
| 403836001 | http://snomed.info/sct | Autosomal recessive hyperimmunoglobulin M syndrome (disorder) |
| 403837005 | http://snomed.info/sct | Wiskott-Aldrich autosomal dominant variant syndrome (disorder) |
| 414029004 | http://snomed.info/sct | Disorder of immune function (disorder) |
| 425835006 | http://snomed.info/sct | Disorder of immune reconstitution (disorder) |
| 426202004 | http://snomed.info/sct | Immune reconstitution syndrome (disorder) |
| 426768001 | http://snomed.info/sct | Engraftment syndrome (disorder) |
| 427167008 | http://snomed.info/sct | Hereditary angioedema with normal C1 esterase inhibitor activity (disorder) |
| 442459007 | http://snomed.info/sct | Combined immunodeficiency disease (disorder) |
| 444547006 | http://snomed.info/sct | Graft versus host disease of skin (disorder) |
| 449187006 | http://snomed.info/sct | Kappa light chain deficiency (disorder) |
| 449384005 | http://snomed.info/sct | Lambda light chain deficiency (disorder) |
| 44940001 | http://snomed.info/sct | Adenosine deaminase deficiency (disorder) |
| 45390000 | http://snomed.info/sct | Severe combined immunodeficiency due to absent interleukin-2 production (disorder) |
| 49555001 | http://snomed.info/sct | Severe combined immunodeficiency due to absent T cell receptor (disorder) |
| 50926003 | http://snomed.info/sct | Job's syndrome (disorder) |
| 55602000 | http://snomed.info/sct | Nezelof's syndrome (disorder) |
| 58034007 | http://snomed.info/sct | Congenital hypergammaglobulinemia (disorder) |
| 702444009 | http://snomed.info/sct | Autoimmune lymphoproliferative syndrome (disorder) |
| 715982006 | http://snomed.info/sct | Severe combined immunodeficiency due to deoxyribonucleic acid cross-link repair protein 1c deficiency (disorder) |
| 716378008 | http://snomed.info/sct | Combined immunodeficiency due to Zeta-chain associated protein kinase 70 deficiency (disorder) |
| 716871006 | http://snomed.info/sct | Severe combined immunodeficiency due to deoxyribonucleic acid dependent protein kinase catalytic subunit deficiency (disorder) |
| 717811007 | http://snomed.info/sct | Combined immunodeficiency due to calcium release activated calcium channel dysfunction (disorder) |
| 718107000 | http://snomed.info/sct | Severe combined immunodeficiency T-cell negative B-cell positive due to janus kinase-3 deficiency (disorder) |
| 71904008 | http://snomed.info/sct | Severe combined immunodeficiency due to absent class II human leukocyte antigens (disorder) |
| 719685004 | http://snomed.info/sct | Absent thumb with short stature and immunodeficiency syndrome (disorder) |
| 719824001 | http://snomed.info/sct | Vici syndrome (disorder) |
| 720345008 | http://snomed.info/sct | Severe T-cell immunodeficiency, congenital alopecia, nail dystrophy syndrome (disorder) |
| 720853005 | http://snomed.info/sct | Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome (disorder) |
| 720986005 | http://snomed.info/sct | Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome (disorder) |
| 721977007 | http://snomed.info/sct | Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome (disorder) |
| 722067005 | http://snomed.info/sct | Severe combined immunodeficiency with hypereosinophilia (disorder) |
| 723995003 | http://snomed.info/sct | Schimke immuno-osseous dysplasia (disorder) |
| 724177005 | http://snomed.info/sct | Ligase 4 syndrome (disorder) |
| 724179008 | http://snomed.info/sct | Laron syndrome with immunodeficiency (disorder) |
| 724275005 | http://snomed.info/sct | Primary immunodeficiency with natural killer cell deficiency and adrenal insufficiency (disorder) |
| 724361001 | http://snomed.info/sct | Hepatic veno-occlusive disease with immunodeficiency syndrome (disorder) |
| 725135004 | http://snomed.info/sct | Combined immunodeficiency due to CD3gamma deficiency (disorder) |
| 725136003 | http://snomed.info/sct | Immunodeficiency by defective expression of human leukocyte antigen class 1 (disorder) |
| 725290000 | http://snomed.info/sct | Combined immunodeficiency due to partial recombination-activating gene 1 deficiency (disorder) |
| 762618008 | http://snomed.info/sct | Bronchiolitis obliterans syndrome due to and after lung transplantation (disorder) |
| 763623001 | http://snomed.info/sct | Severe combined immunodeficiency due to cytidine 5-prime triphosphate synthetase 1 deficiency (disorder) |
| 765145001 | http://snomed.info/sct | T cell negative B cell positive severe combined immunodeficiency due to gamma chain deficiency (disorder) |
| 765188009 | http://snomed.info/sct | Severe combined immunodeficiency due to complete recombination-activating gene 1 and/or recombination-activating gene 2 deficiency (disorder) |
| 766879006 | http://snomed.info/sct | Combined immunodeficiency due to OX40 deficiency (disorder) |
| 766983005 | http://snomed.info/sct | Susceptibility to respiratory infection associated with CD8alpha chain mutation (disorder) |
| 770625006 | http://snomed.info/sct | Combined immunodeficiency with faciooculoskeletal anomalies syndrome (disorder) |
| 771078002 | http://snomed.info/sct | Immunodeficiency due to mannan binding lectin serine peptidase 2 deficiency (disorder) |
| 771309000 | http://snomed.info/sct | Autosomal recessive lymphoproliferative disease (disorder) |
| 771443008 | http://snomed.info/sct | Complement component 3 deficiency (disorder) |
| 771479000 | http://snomed.info/sct | Combined immunodeficiency due to serine/threonine kinase 4 deficiency (disorder) |
| 771515001 | http://snomed.info/sct | Facial dysmorphism, immunodeficiency, livedo, short stature syndrome (disorder) |
| 771517009 | http://snomed.info/sct | Severe combined immunodeficiency due to caspase recruitment domain family member 11 deficiency (disorder) |
| 773404000 | http://snomed.info/sct | Roifman syndrome (disorder) |
| 773488000 | http://snomed.info/sct | Combined immunodeficiency due to mucosa-associated lymphoid tissue lymphoma translocation gene 1 deficiency (disorder) |
| 774211005 | http://snomed.info/sct | Severe dermatitis, multiple allergies, metabolic wasting syndrome (disorder) |
| 778027003 | http://snomed.info/sct | Primary CD59 deficiency (disorder) |
| 782750002 | http://snomed.info/sct | T-cell receptor alpha-beta-positive T-cell deficiency (disorder) |
| 782751003 | http://snomed.info/sct | Severe combined immunodeficiency due to inhibitor of nuclear factor kappa B kinase subunit beta deficiency (disorder) |
| 783007005 | http://snomed.info/sct | Recurrent Neisseria infection due to factor D deficiency (disorder) |
| 783099001 | http://snomed.info/sct | Radiosensitivity, immunodeficiency, dysmorphic features, learning difficulties syndrome (disorder) |
| 783142006 | http://snomed.info/sct | Pancytopenia due to IKAROS family zinc finger 1 mutations (disorder) |
| 783248004 | http://snomed.info/sct | Hyperimmunoglobulin M syndrome with susceptibility to opportunistic infection (disorder) |
| 783249007 | http://snomed.info/sct | Hyperimmunoglobulin M syndrome without susceptibility to opportunistic infection (disorder) |
| 783617001 | http://snomed.info/sct | Severe combined immunodeficiency due to lymphocyte-specific protein-tyrosine kinase deficiency (disorder) |
| 783621008 | http://snomed.info/sct | Immunodeficiency with factor I anomaly (disorder) |
| 783743009 | http://snomed.info/sct | Combined immunodeficiency with granulomatosis (disorder) |
| 784340000 | http://snomed.info/sct | Combined immunodeficiency due to interleukin 21 receptor deficiency (disorder) |
| 789777007 | http://snomed.info/sct | Short-limb skeletal dysplasia with severe combined immunodeficiency (disorder) |
| 7990002 | http://snomed.info/sct | Immunoglobulinemia with isolated somatotropin deficiency (disorder) |
| 81166004 | http://snomed.info/sct | Properdin deficiency disease (disorder) |
| 82286005 | http://snomed.info/sct | Hyperimmunoglobulin M syndrome (disorder) |
| 82966003 | http://snomed.info/sct | Hereditary angioedema (disorder) |
| 829973009 | http://snomed.info/sct | Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis (disorder) |
| 846606007 | http://snomed.info/sct | Graft versus host disease of liver (disorder) |
| 88714009 | http://snomed.info/sct | Transient hypogammaglobulinemia of infancy (disorder) |
Produced 08 Sep 2023