| Source | us.nlm.vsac#0.11.0:null (v4.0.1) |
| resourceType | ValueSet |
| id | 2.16.840.1.113883.3.464.1003.120.11.1001 |
| canonical | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.464.1003.120.11.1001 |
| version | 20230208 |
| status | active |
| publisher | NCQA PHEMUR |
| name | DisordersOfTheImmuneSystem |
| title | Disorders of the Immune System |
| date | 2023-02-08T01:02:57-05:00 |
| Usages |
|
This value set contains 105 concepts
| Code | System | Display |
| 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) |
| 1197361002 | http://snomed.info/sct | Autoimmune lymphoproliferative syndrome due to cytotoxic T-lymphocyte associated protein 4 haploinsufficiency (disorder) |
| 1197362009 | http://snomed.info/sct | Signal transducer and activator of transcription 3-related early-onset multisystem autoimmune disease (disorder) |
| 121121000119106 | http://snomed.info/sct | Acute graft-versus-host reaction following bone marrow transplant (disorder) |
| 121131000119109 | http://snomed.info/sct | Chronic graft versus host disease after transplantation of bone marrow (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) |
| 23238000 | http://snomed.info/sct | Common variable agammaglobulinemia (disorder) |
| 234532001 | http://snomed.info/sct | Immunodeficiency disorder (disorder) |
| 234562007 | http://snomed.info/sct | Anti-protein antibody deficiency (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) |
| 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) |
| 263661007 | http://snomed.info/sct | Complement 5 dysfunction (disorder) |
| 36070007 | http://snomed.info/sct | Wiskott-Aldrich syndrome (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) |
| 426202004 | http://snomed.info/sct | Immune reconstitution 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) |
| 55602000 | http://snomed.info/sct | Nezelof's syndrome (disorder) |
| 702444009 | http://snomed.info/sct | Autoimmune lymphoproliferative syndrome (disorder) |
| 719156006 | http://snomed.info/sct | X-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome (disorder) |
| 720853005 | http://snomed.info/sct | Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome (disorder) |
| 722067005 | http://snomed.info/sct | Severe combined immunodeficiency with hypereosinophilia (disorder) |
| 724361001 | http://snomed.info/sct | Hepatic veno-occlusive disease with immunodeficiency syndrome (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) |
| 765188009 | http://snomed.info/sct | Severe combined immunodeficiency due to complete recombination-activating gene 1 and/or recombination-activating gene 2 deficiency (disorder) |
| 771078002 | http://snomed.info/sct | Immunodeficiency due to mannan binding lectin serine peptidase 2 deficiency (disorder) |
| 771443008 | http://snomed.info/sct | Complement component 3 deficiency (disorder) |
| 778027003 | http://snomed.info/sct | Primary CD59 deficiency (disorder) |
| 783007005 | http://snomed.info/sct | Recurrent Neisseria infection due to factor D deficiency (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) |
| 789777007 | http://snomed.info/sct | Short-limb skeletal dysplasia with severe combined immunodeficiency (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) |
| 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