Permanent Immunosuppression (SNOMED)
Codelist metadata
-
Coding system
- SNOMED CT
-
Coding system release
- unknown
-
Organisation
- OpenSAFELY
-
Codelist ID
- opensafely/permanent-immunosuppression-snomed
-
Version Tag
- 2020-06-02
-
Version ID
- 55914b31
Versions
About
Description
Automatically-generated equivalent of Permanent Immunosuppression
Methodology
See code on GitHub
Codelists are developed by a broad community of users for individual study purposes, which may or may not meet the needs of other studies. They should not be thought of as universal definitions of a particular condition.
We don't offer any guarantees about what they do or don't identify. Users should carefully check that any codelist meets their needs, and seek clinical input where appropriate.
| id | name | active | notes |
|---|---|---|---|
| 267459007 | Deficiencies of humoral immunity (finding) | y | direct mapping |
| 191002000 | Major histocompatibility complex class II deficiency (disorder) | y | direct mapping |
| 191338000 | Primary splenic neutropenia (disorder) | y | direct mapping |
| 111584000 | Reticular dysgenesis (disorder) | y | direct mapping |
| 248693006 | Chronic idiopathic neutropenia (disorder) | y | direct mapping |
| 65880007 | X-linked agammaglobulinemia (disorder) | y | direct mapping |
| 190993005 | Autosomal recessive severe combined immunodeficiency (disorder) | y | direct mapping |
| 82286005 | Hyperimmunoglobulin M syndrome (disorder) | y | direct mapping |
| 240718005 | Chronic localized mucocutaneous candidiasis (disorder) | y | direct mapping |
| 267543009 | Functional disorders of polymorphonuclear neutrophils (disorder) | y | direct mapping |
| 234609006 | Complement 5 deficiency (disorder) | y | direct mapping |
| 50926003 | Job's syndrome (disorder) | y | direct mapping |
| 234631003 | Immunodeficiency with major anomalies (disorder) | y | direct mapping |
| 191013002 | Common variable immunodeficiency with autoantibodies to B- or T-cells (disorder) | y | direct mapping |
| 234590006 | Gluthathione peroxidase deficiency (disorder) | y | direct mapping |
| 71904008 | Severe combined immunodeficiency due to absent class II human leukocyte antigens (disorder) | y | direct mapping |
| 234578009 | Defective phagocytic cell opsonization (disorder) | y | direct mapping |
| 703538003 | Mannose-binding lectin deficiency (disorder) | y | direct mapping |
| 234619000 | Hereditary C1 esterase inhibitor deficiency - deficient factor (disorder) | y | direct mapping |
| 235073000 | Familial chronic mucocutaneous candidiasis (disorder) | y | direct mapping |
| 234605000 | Factor B deficiency (disorder) | y | direct mapping |
| 234533006 | X-linked agammaglobulinemia with growth hormone deficiency (disorder) | y | direct mapping |
| 234539005 | Immunoglobulin heavy chain deficiency (disorder) | y | direct mapping |
| 234607008 | Factor D deficiency (disorder) | y | direct mapping |
| 234547005 | Combined immunoglobulin G2 and G4 deficiency (disorder) | y | direct mapping |
| 234628004 | Complement receptor deficiency (disorder) | y | direct mapping |
| 234571003 | Warts, hypogammaglobulinemia, infections, and myelokathexis (disorder) | y | direct mapping |
| 302874002 | Phagocytic cell dysfunction (disorder) | y | direct mapping |
| 234534000 | Autosomal agammaglobulinemia with absent B-cells (disorder) | y | direct mapping |
| 119249001 | Agammaglobulinemia (finding) | y | direct mapping |
| 191001007 | Major histocompatibility complex class I deficiency (disorder) | y | direct mapping |
| 111396008 | Chédiak-Higashi syndrome (disorder) | y | direct mapping |
| 77121009 | X-linked lymphoproliferative syndrome (disorder) | y | direct mapping |
| 398055000 | T-lymphocyte deficiency (finding) | y | direct mapping |
| 190997006 | Severe combined immunodeficiency with low T- and B-cell numbers (disorder) | y | direct mapping |
| 767263007 | 22q11.2 deletion syndrome (disorder) | y | direct mapping |
| 234623008 | Complement 4 binding protein deficiency (disorder) | y | direct mapping |
| 234550008 | Immunoglobulin G1 deficiency (disorder) | y | direct mapping |
| 403836001 | Autosomal recessive hyperimmunoglobulin M syndrome (disorder) | y | direct mapping |
| 234568006 | Chronic mucocutaneous candidiasis (disorder) | y | direct mapping |
| 89655007 | Congenital neutropenia (disorder) | y | direct mapping |
| 234551007 | Immunoglobulin A1 deficiency (disorder) | y | direct mapping |
| 234636008 | Monosomy 22 and absence of immunoglobulin A (disorder) | y | direct mapping |
| 234416002 | X-linked hypogammaglobulinemia (disorder) | y | direct mapping |
| 304576008 | Metaphyseal chondrodysplasia, McKusick type with associated immunodeficiency (disorder) | y | direct mapping |
| 190995003 | Thymic aplasia or dysplasia with immunodeficiency (disorder) | y | direct mapping |
| 234583001 | Leukocyte adhesion deficiency - type 2 (disorder) | y | direct mapping |
| 234548000 | Immunoglobulin G3 deficiency (disorder) | y | direct mapping |
| 234579001 | Mannan-binding protein deficiency (disorder) | y | direct mapping |
| 234582006 | Leukocyte adhesion deficiency - type 1 (disorder) | y | direct mapping |
| 234615006 | Complement 8 beta chain dysfunction (disorder) | y | direct mapping |
| 37548006 | Hypopigmentation-immunodeficiency disease (disorder) | y | direct mapping |
| 234597009 | Complement 1r deficiency (disorder) | y | direct mapping |
| 449187006 | Kappa light chain deficiency (disorder) | y | direct mapping |
| 58606001 | Primary immune deficiency disorder (disorder) | y | direct mapping |
| 426202004 | Immune reconstitution syndrome (disorder) | y | direct mapping |
| 234554004 | Secretory piece deficiency (disorder) | y | direct mapping |
| 44940001 | Adenosine deaminase deficiency (disorder) | y | direct mapping |
| 234544003 | Immunoglobulin subclass deficiency (disorder) | y | direct mapping |
| 234430007 | CR3-receptor deficiency (disorder) | y | direct mapping |
| 55602000 | Nezelof's syndrome (disorder) | y | direct mapping |
| 234620006 | Hereditary C1 esterase inhibitor deficiency - dysfunctional factor (disorder) | y | direct mapping |
| 234549008 | Immunoglobulin G4 deficiency (disorder) | y | direct mapping |
| 31323000 | Severe combined immunodeficiency disease (disorder) | y | direct mapping |
| 234599007 | Complement 2 deficiency (disorder) | y | direct mapping |
| 190981001 | Selective immunoglobulin G deficiency (disorder) | y | direct mapping |
| 234625001 | Homologous restriction factor deficiency (disorder) | y | direct mapping |
| 234612009 | Complement 7 deficiency (disorder) | y | direct mapping |
| 234638009 | Microcephaly, normal intelligence and immunodeficiency (disorder) | y | direct mapping |
| 234584007 | Tuftsin deficiency (disorder) | y | direct mapping |
| 234433009 | Myeloperoxidase deficiency (disorder) | y | direct mapping |
| 234635007 | Chromosome 22 abnormalities with hypogammaglobulinemia (disorder) | y | direct mapping |
| 234616007 | Complement 8 alpha-gamma deficiency (disorder) | y | direct mapping |
| 234538002 | Hyperimmunoglobulin D with periodic fever (finding) | y | direct mapping |
| 234632005 | Immunodeficiency associated with chromosomal abnormality (disorder) | y | direct mapping |
| 403835002 | X-linked hyper-immunoglobulin M syndrome (disorder) | y | direct mapping |
| 234546001 | Immunoglobulin G2 deficiency (disorder) | y | direct mapping |
| 234629007 | Complement receptor 1 deficiency (disorder) | y | direct mapping |
| 234570002 | Severe combined immunodeficiency with maternofetal engraftment (disorder) | y | direct mapping |
| 234367000 | Pancytopenia with pancreatitis (disorder) | y | direct mapping |
| 191011000 | Common variable immunodeficiency with predominant abnormalities of B-cell numbers and functions (disorder) | y | direct mapping |
| 68504005 | Ataxia-telangiectasia syndrome (disorder) | y | direct mapping |
| 234598004 | Complement 1s deficiency (disorder) | y | direct mapping |
| 81166004 | Properdin deficiency disease (disorder) | y | direct mapping |
| 3439009 | Severe combined immunodeficiency due to absent peripheral T cell maturation (disorder) | y | direct mapping |
| 234435002 | Hereditary hypersegmentation (disorder) | y | direct mapping |
| 267460002 | Congenital hypogammaglobulinemia (finding) | y | direct mapping |
| 234434003 | Alders syndrome (disorder) | y | direct mapping |
| 234577004 | Lipochrome histiocytosis - familial (disorder) | y | direct mapping |
| 234613004 | Combined complement 6 and 7 deficiencies (disorder) | y | direct mapping |
| 234555003 | Defective immunoglobulin glycosylation (disorder) | y | direct mapping |
| 190979003 | Selective immunoglobulin A deficiency (disorder) | y | direct mapping |
| 25109007 | Lymphopenic agammaglobulinemia - short-limbed dwarfism syndrome (disorder) | y | direct mapping |
| 191018006 | Lymphocyte function antigen-1 defect (disorder) | y | direct mapping |
| 66876008 | Lambda light chain disease (disorder) | y | direct mapping |
| 24974008 | Myelokathexis (disorder) | y | direct mapping |
| 234594002 | Complement 1q deficiency (disorder) | y | direct mapping |
| 191347008 | Cyclical neutropenia (disorder) | y | direct mapping |
| 234587000 | Neutrophil lactoferrin deficiency (disorder) | y | direct mapping |
| 234608003 | Terminal component deficiency (disorder) | y | direct mapping |
| 234542004 | Selective immunoglobulin M and immunoglobulin A deficiency (disorder) | y | direct mapping |
| 234595001 | Complement 1q beta chain deficiency (disorder) | y | direct mapping |
| 60743005 | Purine-nucleoside phosphorylase deficiency (disorder) | y | direct mapping |
| 234618008 | Complement regulatory factor defect (disorder) | y | direct mapping |
| 234634006 | Chromosome 18 syndromes and antibody deficiency (disorder) | y | direct mapping |
| 234627009 | Anaphylotoxin inactivator deficiency (disorder) | y | direct mapping |
| 234611002 | Complement 6 deficiency (disorder) | y | direct mapping |
| 234603007 | Complement 3 deficiency (disorder) | y | direct mapping |
| 234586009 | Leukocyte glucose-6-phosphate dehydrogenase deficiency (disorder) | y | direct mapping |
| 234637004 | Deletion of X-chromosome and hypogammaglobulinemia (disorder) | y | direct mapping |
| 234621005 | Factor I deficiency (disorder) | y | direct mapping |
| 191008001 | Immunodeficiency following hereditary defective response to Epstein-Barr virus (disorder) | y | direct mapping |
| 387759001 | Chronic granulomatous disease (disorder) | y | direct mapping |
| 190980000 | Selective immunoglobulin M deficiency (disorder) | y | direct mapping |
| 234576008 | Chronic familial neutropenia (disorder) | y | direct mapping |
| 234585008 | Defective phagocytic cell killing (disorder) | y | direct mapping |
| 234484005 | May-Hegglin anomaly (disorder) | y | direct mapping |
| 263661007 | Complement 5 dysfunction (disorder) | y | direct mapping |
| 234614005 | Complement 8 beta chain deficiency (disorder) | y | direct mapping |
| 234633000 | Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency (disorder) | y | direct mapping |
| 234431006 | Specific granule deficiency (disorder) | y | direct mapping |
| 234640004 | 18-p syndrome with associated immunodeficiency (disorder) | y | direct mapping |
| 190996002 | Severe combined immunodeficiency with reticular dysgenesis (disorder) | y | direct mapping |
| 234641000 | Immunodeficiency associated with multiple organ system abnormalities (disorder) | y | direct mapping |
| 234588005 | Neutrophil secondary granule deficiency (disorder) | y | direct mapping |
| 234593008 | Classical complement pathway abnormality (disorder) | y | direct mapping |
| 234602002 | Complement 4B deficiency (disorder) | y | direct mapping |
| 234604001 | Alternative pathway deficiency (disorder) | y | direct mapping |
| 4434006 | Bloom syndrome (disorder) | y | direct mapping |
| 234553005 | Immunoglobulin-associated molecule deficiency (disorder) | y | direct mapping |
| 190998001 | Severe combined immunodeficiency with low or normal B-cell numbers (disorder) | y | direct mapping |
| 23238000 | Common variable agammaglobulinemia (disorder) | y | direct mapping |
| 183023001 | Transplant immunosuppression (procedure) | y | direct mapping |
| 234630002 | Complement receptor 3 deficiency (disorder) | y | direct mapping |
| 240717000 | Familial chronic mucocutaneous candidiasis - late onset type (disorder) | y | direct mapping |
| 234600005 | Complement 4 deficiency (disorder) | y | direct mapping |
| 234580003 | Defective phagocytic cell chemotaxis (disorder) | y | direct mapping |
| 234424007 | Metabolic neutropenia (disorder) | y | direct mapping |
| 234617003 | Complement 9 deficiency (disorder) | y | direct mapping |
| 398250003 | Familial hemophagocytic lymphohistiocytosis (disorder) | y | direct mapping |
| 191012007 | Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder) | y | direct mapping |
| 398293003 | Cellular immune defect (finding) | y | direct mapping |
| 234589002 | Glutathione synthetase deficiency (disorder) | y | direct mapping |
| 234596000 | Complement 1q dysfunction (disorder) | y | direct mapping |
| 234626000 | Complement 5a inhibitor deficiency (disorder) | y | direct mapping |
| 234552000 | Immunoglobulin A2 deficiency (disorder) | y | direct mapping |
| 240719002 | Chronic diffuse mucocutaneous candidiasis (disorder) | y | direct mapping |
| 89454001 | Shwachman syndrome (disorder) | y | direct mapping |
| 234591005 | Combined phagocytic defect (disorder) | y | direct mapping |
| 234624002 | Decay accelerating factor deficiency (disorder) | y | direct mapping |
| 234532001 | Immunodeficiency disorder (disorder) | y | direct mapping |
| 91918005 | Congenital absence of thymus (disorder) | y | direct mapping |
| 234581004 | Defective phagocytic cell adhesion (disorder) | y | direct mapping |
| 234425008 | Autoimmune neutropenia (disorder) | y | direct mapping |
| 234543009 | Immunoglobulin light chain deficiency (disorder) | y | direct mapping |
| 234639001 | Triple X syndrome, epilepsy, and hypogammaglobulinemia (disorder) | y | direct mapping |
| 71436005 | Lazy leukocyte syndrome (disorder) | y | direct mapping |
| 36070007 | Wiskott-Aldrich syndrome (disorder) | y | direct mapping |
| 254067002 | Immuno-osseous dysplasia (disorder) | y | direct mapping |
| 82966003 | Hereditary angioedema (disorder) | y | direct mapping |
| 234601009 | Complement 4A deficiency (disorder) | y | direct mapping |
| 234535004 | Selective immunoglobulin dysfunction (finding) | y | direct mapping |
| 234622003 | Factor H deficiency (disorder) | y | direct mapping |
| 77358003 | Congenital leukocyte adherence deficiency (disorder) | y | descendant of concept mapped from leaf |
| 721877008 | Mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency (disorder) | y | descendant of concept mapped from leaf |
| 29260007 | Immunoglobulin A deficiency (disorder) | y | descendant of concept mapped from leaf |
| 39674000 | Familial C3B inhibitor deficiency syndrome (disorder) | y | descendant of concept mapped from leaf |
| 725290000 | Combined immunodeficiency due to partial recombination-activating gene 1 deficiency (disorder) | y | descendant of concept mapped from leaf |
| 724641002 | Primary hemophagocytic lymphohistiocytosis (disorder) | y | descendant of concept mapped from leaf |
| 719824001 | Vici syndrome (disorder) | y | descendant of concept mapped from leaf |
| 417167007 | Immunoglobulin deficiency (disorder) | y | descendant of concept mapped from leaf |
| 129639005 | Hereditary neutrophilia (disorder) | y | descendant of concept mapped from leaf |
| 720345008 | Severe T-cell immunodeficiency, congenital alopecia, nail dystrophy syndrome (disorder) | y | descendant of concept mapped from leaf |
| 724275005 | Primary immunodeficiency with natural killer cell deficiency and adrenal insufficiency (disorder) | y | descendant of concept mapped from leaf |
| 10746341000119109 | Acquired immune deficiency syndrome complicating childbirth (disorder) | y | descendant of concept mapped from leaf |
| 234560004 | Anti-meningococcal polysaccharide A antibody deficiency (disorder) | y | descendant of concept mapped from leaf |
| 78378009 | Isoimmune neutropenia (disorder) | y | descendant of concept mapped from leaf |
| 725432008 | Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency (disorder) | y | descendant of concept mapped from leaf |
| 723508002 | RAS-associated autoimmune leukoproliferative disease (disorder) | y | descendant of concept mapped from leaf |
| 449853003 | Interleukin-12 deficiency (disorder) | y | descendant of concept mapped from leaf |
| 63484008 | Drug-induced neutrophilia (disorder) | y | descendant of concept mapped from leaf |
| 765327005 | Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome (disorder) | y | descendant of concept mapped from leaf |
| 703525006 | Anhidrotic ectodermal dysplasia with immune deficiency (disorder) | y | descendant of concept mapped from leaf |
| 737307003 | Natural-killer cell deficiency (disorder) | y | descendant of concept mapped from leaf |
| 766983005 | Susceptibility to respiratory infection associated with CD8alpha chain mutation (disorder) | y | descendant of concept mapped from leaf |
| 764946008 | Constitutional mismatch repair deficiency syndrome (disorder) | y | descendant of concept mapped from leaf |
| 718232007 | Pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 (disorder) | y | descendant of concept mapped from leaf |
| 234574006 | Disorder of phagocytic cell number (disorder) | y | descendant of concept mapped from leaf |
| 103080003 | Immunodeficiency secondary to radiation therapy (disorder) | y | descendant of concept mapped from leaf |
| 363009005 | Complement component deficiency (disorder) | y | descendant of concept mapped from leaf |
| 711480000 | Activated PI3K-delta syndrome (disorder) | y | descendant of concept mapped from leaf |
| 234562007 | Anti-protein antibody deficiency (disorder) | y | descendant of concept mapped from leaf |
| 417672002 | Granulocytopenic disorder (disorder) | y | descendant of concept mapped from leaf |
| 421312009 | Agranulocytosis associated with acquired immunodeficiency syndrome (disorder) | y | descendant of concept mapped from leaf |
| 735435002 | Constitutional neutrophilia (disorder) | y | descendant of concept mapped from leaf |
| 709465004 | Periodontitis co-occurrent with Chédiak-Higashi syndrome (disorder) | y | descendant of concept mapped from leaf |
| 55444004 | Transient neonatal neutropenia (disorder) | y | descendant of concept mapped from leaf |
| 406565005 | CD4 T lymphocyte deficiency (disorder) | y | descendant of concept mapped from leaf |
| 709608008 | Periodontitis co-occurrent with acquired neutropenia (disorder) | y | descendant of concept mapped from leaf |
| 111587007 | Severe combined immunodeficiency due to absent interleukin-2 receptor (disorder) | y | descendant of concept mapped from leaf |
| 33286000 | Secondary immune deficiency disorder (disorder) | y | descendant of concept mapped from leaf |
| 722290008 | Autoimmune lymphoproliferative syndrome with recurrent viral infection (disorder) | y | descendant of concept mapped from leaf |
| 725137007 | Neutropenia, monocytopenia, deafness syndrome (disorder) | y | descendant of concept mapped from leaf |
| 103077004 | Immunodeficiency secondary to neoplasm (disorder) | y | descendant of concept mapped from leaf |
| 111585004 | Neutropenia associated with autoimmune disease (disorder) | y | descendant of concept mapped from leaf |
| 77330006 | Chronic granulomatous disease, type II (disorder) | y | descendant of concept mapped from leaf |
| 403837005 | Wiskott-Aldrich autosomal dominant variant syndrome (disorder) | y | descendant of concept mapped from leaf |
| 58034007 | Congenital hypergammaglobulinemia (disorder) | y | descendant of concept mapped from leaf |
| 414850009 | Neutrophilia (disorder) | y | descendant of concept mapped from leaf |
| 350353007 | De Vaal's syndrome (disorder) | y | descendant of concept mapped from leaf |
| 722281001 | Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome (disorder) | y | descendant of concept mapped from leaf |
| 735536003 | Adult-onset immunodeficiency (disorder) | y | descendant of concept mapped from leaf |
| 234642007 | Age-related immunodeficiency (disorder) | y | descendant of concept mapped from leaf |
| 427167008 | Hereditary angioedema with normal C1 esterase inhibitor activity (disorder) | y | descendant of concept mapped from leaf |
| 62479008 | Acquired immune deficiency syndrome (disorder) | y | descendant of concept mapped from leaf |
| 402792003 | T-lymphocyte immunodeficiency (disorder) | y | descendant of concept mapped from leaf |
| 724015007 | Pyogenic arthritis, pyoderma gangrenosum, acne syndrome (disorder) | y | descendant of concept mapped from leaf |
| 234437005 | Hemophagocytic lymphohistiocytosis (disorder) | y | descendant of concept mapped from leaf |
| 722067005 | Severe combined immunodeficiency with hypereosinophilia (disorder) | y | descendant of concept mapped from leaf |
| 234573000 | Phagocytic cell defect (disorder) | y | descendant of concept mapped from leaf |
| 234563002 | Anti-staphylococcal antibody deficiency (disorder) | y | descendant of concept mapped from leaf |
| 29272001 | Chronic granulomatous disease, type I (disorder) | y | descendant of concept mapped from leaf |
| 717811007 | Combined immunodeficiency due to calcium release activated calcium channel dysfunction (disorder) | y | descendant of concept mapped from leaf |
| 449384005 | Lambda light chain deficiency (disorder) | y | descendant of concept mapped from leaf |
| 351287008 | Reticular dysgenesis with congenital aleukocytosis (disorder) | y | descendant of concept mapped from leaf |
| 718230004 | Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency (disorder) | y | descendant of concept mapped from leaf |
| 724276006 | X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome (disorder) | y | descendant of concept mapped from leaf |
| 719685004 | Absent thumb with short stature and immunodeficiency syndrome (disorder) | y | descendant of concept mapped from leaf |
| 26252007 | Chronic granulomatous disease, type IIA (disorder) | y | descendant of concept mapped from leaf |
| 722288007 | Autoimmune enteropathy and endocrinopathy with susceptibility to chronic infection syndrome (disorder) | y | descendant of concept mapped from leaf |
| 426800001 | Febrile granulocytopenia (disorder) | y | descendant of concept mapped from leaf |
| 720520009 | Attenuated Chédiak-Higashi syndrome (disorder) | y | descendant of concept mapped from leaf |
| 46359005 | Neutropenia associated with infectious disease (disorder) | y | descendant of concept mapped from leaf |
| 716871006 | Severe combined immunodeficiency due to deoxyribonucleic acid dependent protein kinase catalytic subunit deficiency (disorder) | y | descendant of concept mapped from leaf |
| 724361001 | Hepatic veno-occlusive disease with immunodeficiency syndrome (disorder) | y | descendant of concept mapped from leaf |
| 402791005 | B-lymphocyte immunodeficiency (disorder) | y | descendant of concept mapped from leaf |
| 47144000 | Acute neutrophilia (disorder) | y | descendant of concept mapped from leaf |
| 763668009 | Lichtenstein syndrome (disorder) | y | descendant of concept mapped from leaf |
| 56918001 | Dose-related drug-induced neutropenia (disorder) | y | descendant of concept mapped from leaf |
| 735434003 | Acquired neutrophilia (disorder) | y | descendant of concept mapped from leaf |
| 763623001 | Severe combined immunodeficiency due to cytidine 5-prime triphosphate synthetase 1 deficiency (disorder) | y | descendant of concept mapped from leaf |
| 723995003 | Schimke immuno-osseous dysplasia (disorder) | y | descendant of concept mapped from leaf |
| 234645009 | Drug-induced immunodeficiency (disorder) | y | descendant of concept mapped from leaf |
| 234559009 | Anti-pneumococcal polysaccharide antibody deficiency (disorder) | y | descendant of concept mapped from leaf |
| 765145001 | T cell negative B cell positive severe combined immunodeficiency due to gamma chain deficiency (disorder) | y | descendant of concept mapped from leaf |
| 724177005 | Ligase 4 syndrome (disorder) | y | descendant of concept mapped from leaf |
| 725151007 | Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency (disorder) | y | descendant of concept mapped from leaf |
| 709535007 | Periodontitis co-occurrent with infantile genetic agranulocytosis (disorder) | y | descendant of concept mapped from leaf |
| 234565009 | Immunoglobulin hypercatabolism (disorder) | y | descendant of concept mapped from leaf |
| 715982006 | Severe combined immunodeficiency due to deoxyribonucleic acid cross-link repair protein 1c deficiency (disorder) | y | descendant of concept mapped from leaf |
| 765188009 | Severe combined immunodeficiency due to complete recombination-activating gene 1 and/or recombination-activating gene 2 deficiency (disorder) | y | descendant of concept mapped from leaf |
| 726078000 | Sporadic Blau syndrome (disorder) | y | descendant of concept mapped from leaf |
| 247860002 | Familial neutropenia (disorder) | y | descendant of concept mapped from leaf |
| 80369006 | Chronic neutrophilia (disorder) | y | descendant of concept mapped from leaf |
| 10838971000119103 | Immunodeficiency caused by long term therapeutic use of drug (disorder) | y | descendant of concept mapped from leaf |
| 721903007 | Microcephaly, hypogammaglobulinemia, abnormal immunity syndrome (disorder) | y | descendant of concept mapped from leaf |
| 713530002 | Agranulocytosis co-occurrent with human immunodeficiency virus infection (disorder) | y | descendant of concept mapped from leaf |
| 234426009 | Corticosteroid-induced neutrophilia (disorder) | y | descendant of concept mapped from leaf |
| 719814009 | X-linked mendelian susceptibility to mycobacterial disease (disorder) | y | descendant of concept mapped from leaf |
| 234557006 | Anti-polysaccharide antibody deficiency (disorder) | y | descendant of concept mapped from leaf |
| 721876004 | Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 2 deficiency (disorder) | y | descendant of concept mapped from leaf |
| 234643002 | Transient immunodeficiency of infancy (disorder) | y | descendant of concept mapped from leaf |
| 767658000 | Neutropenia due to and following chemotherapy (disorder) | y | descendant of concept mapped from leaf |
| 234541006 | Selective immunoglobulin D deficiency (disorder) | y | descendant of concept mapped from leaf |
| 725431001 | Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency (disorder) | y | descendant of concept mapped from leaf |
| 402483002 | Immunodeficiency with multicarboxylase deficiency (disorder) | y | descendant of concept mapped from leaf |
| 129642004 | Chronic idiopathic immunoneutropenia in adults (disorder) | y | descendant of concept mapped from leaf |
| 723386002 | Mendelian susceptibility to mycobacterial disease due to partial signal transducer and activator of transcription 1 deficiency (disorder) | y | descendant of concept mapped from leaf |
| 129640007 | Benign granulocytopenia in childhood (disorder) | y | descendant of concept mapped from leaf |
| 234566005 | Familial immunoglobulin hypercatabolism (disorder) | y | descendant of concept mapped from leaf |
| 12631000119106 | Immunoglobulin G deficiency (disorder) | y | descendant of concept mapped from leaf |
| 105601003 | Quantitative disorder of neutrophils (disorder) | y | descendant of concept mapped from leaf |
| 24181002 | Aplasia of thymus gland with immunodeficiency (disorder) | y | descendant of concept mapped from leaf |
| 3902000 | Non dose-related drug-induced neutropenia (disorder) | y | descendant of concept mapped from leaf |
| 36980009 | Severe combined immunodeficiency due to absent adenosine deaminase (disorder) | y | descendant of concept mapped from leaf |
| 707152007 | Phagocytic immunodeficiency (disorder) | y | descendant of concept mapped from leaf |
| 22406001 | Severe combined immunodeficiency due to absent lymphoid stem cells (disorder) | y | descendant of concept mapped from leaf |
| 103078009 | Immunodeficiency secondary to trauma (disorder) | y | descendant of concept mapped from leaf |
| 725135004 | Combined immunodeficiency due to CD3gamma deficiency (disorder) | y | descendant of concept mapped from leaf |
| 234561000 | Anti-meningococcal polysaccharide C antibody deficiency (disorder) | y | descendant of concept mapped from leaf |
| 129643009 | Chronic hypoplastic neutropenia (disorder) | y | descendant of concept mapped from leaf |
| 363040003 | Congenital immunodeficiency involving the hematopoietic system (disorder) | y | descendant of concept mapped from leaf |
| 45390000 | Severe combined immunodeficiency due to absent interleukin-2 production (disorder) | y | descendant of concept mapped from leaf |
| 276628009 | Chloramphenicol-induced neutropenia (disorder) | y | descendant of concept mapped from leaf |
| 76243000 | Chronic granulomatous disease, type IVA (disorder) | y | descendant of concept mapped from leaf |
| 720853005 | Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome (disorder) | y | descendant of concept mapped from leaf |
| 718107000 | Severe combined immunodeficiency T-cell negative B-cell positive due to janus kinase-3 deficiency (disorder) | y | descendant of concept mapped from leaf |
| 234556002 | Specific antibody deficiency (disorder) | y | descendant of concept mapped from leaf |
| 723334006 | Immunodeficiency due to mutation of FAS-associated protein with death domain gene (disorder) | y | descendant of concept mapped from leaf |
| 766705006 | Immunodeficiency due to ficolin 3 deficiency (disorder) | y | descendant of concept mapped from leaf |
| 710735009 | Periodontitis co-occurrent with leukocyte adhesion deficiency (disorder) | y | descendant of concept mapped from leaf |
| 14333004 | Alloimmune neonatal neutropenia (disorder) | y | descendant of concept mapped from leaf |
| 234564008 | Primary immunoglobulin catabolism abnormality (disorder) | y | descendant of concept mapped from leaf |
| 47318007 | Drug-induced neutropenia (disorder) | y | descendant of concept mapped from leaf |
| 18827005 | Complement abnormality (disorder) | y | descendant of concept mapped from leaf |
| 716869006 | Mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency (disorder) | y | descendant of concept mapped from leaf |
| 409089005 | Febrile neutropenia (disorder) | y | descendant of concept mapped from leaf |
| 442459007 | Combined immunodeficiency disease (disorder) | y | descendant of concept mapped from leaf |
| 36138009 | Congenital immunodeficiency disease (disorder) | y | descendant of concept mapped from leaf |
| 41814009 | Neutropenia with dysgranulopoiesis (disorder) | y | descendant of concept mapped from leaf |
| 303011007 | Neutropenic disorder (disorder) | y | descendant of concept mapped from leaf |
| 48119005 | Dysplasia of thymus gland with immunodeficiency (disorder) | y | descendant of concept mapped from leaf |
| 103079001 | Immunodeficiency caused by corticosteroid (disorder) | y | descendant of concept mapped from leaf |
| 7990002 | Immunoglobulinemia with isolated somatotropin deficiency (disorder) | y | descendant of concept mapped from leaf |
| 24419001 | Disorder of complement (disorder) | y | descendant of concept mapped from leaf |
| 21527007 | Chronic granulomatous disease, type IV (disorder) | y | descendant of concept mapped from leaf |
| 88714009 | Transient hypogammaglobulinemia of infancy (disorder) | y | descendant of concept mapped from leaf |
| 82317007 | Chronic granulomatous disease, type III (disorder) | y | descendant of concept mapped from leaf |
| 723443003 | Neutrophil immunodeficiency syndrome (disorder) | y | descendant of concept mapped from leaf |
| 725150008 | Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency (disorder) | y | descendant of concept mapped from leaf |
| 768560008 | Melanoma differentiation-associated gene 5 deficiency (disorder) | y | descendant of concept mapped from leaf |
| 718717004 | Primary immunodeficiency syndrome due to p14 deficiency (disorder) | y | descendant of concept mapped from leaf |
| 234558001 | Anti-haemophilus influenzae B polysaccharide antibody deficiency (disorder) | y | descendant of concept mapped from leaf |
| 718882006 | X-linked severe congenital neutropenia (disorder) | y | descendant of concept mapped from leaf |
| 710926008 | Periodontitis co-occurrent with familial neutropenia (disorder) | y | descendant of concept mapped from leaf |
| 763713000 | Idiopathic CD4 lymphocytopenia (disorder) | y | descendant of concept mapped from leaf |
| 234540007 | Selective immunoglobulin E deficiency (disorder) | y | descendant of concept mapped from leaf |
| 716378008 | Combined immunodeficiency due to Zeta-chain associated protein kinase 70 deficiency (disorder) | y | descendant of concept mapped from leaf |
| 103081004 | Immunodeficiency secondary to chemotherapy (disorder) | y | descendant of concept mapped from leaf |
| 699861000 | Familial granulomatous inflammatory arthritis, dermatitis and uveitis (disorder) | y | descendant of concept mapped from leaf |
| 764858009 | Isolated agammaglobulinemia (disorder) | y | descendant of concept mapped from leaf |
| 267540007 | Neutropenia caused by irradiation (disorder) | y | descendant of concept mapped from leaf |
| 719156006 | X-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome (disorder) | y | descendant of concept mapped from leaf |
| 416729007 | Neutropenia associated with acquired immunodeficiency syndrome (disorder) | y | descendant of concept mapped from leaf |
| 234436001 | Hemolytic erythrophagocytic syndrome (disorder) | y | descendant of concept mapped from leaf |
| 766879006 | Combined immunodeficiency due to OX40 deficiency (disorder) | y | descendant of concept mapped from leaf |
| 129641006 | Chronic benign neutropenia of childhood (disorder) | y | descendant of concept mapped from leaf |
| 720986005 | Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome (disorder) | y | descendant of concept mapped from leaf |
| 105602005 | Quantitative abnormality of granulocytes (disorder) | y | descendant of concept mapped from leaf |
| 724179008 | Laron syndrome with immunodeficiency (disorder) | y | descendant of concept mapped from leaf |
| 362993009 | Autosomal recessive severe combined immunodeficiency disease (disorder) | y | descendant of concept mapped from leaf |
| 70349007 | Pseudoneutrophilia (disorder) | y | descendant of concept mapped from leaf |
| 276576000 | Neutropenia of the small for gestational age baby (disorder) | y | descendant of concept mapped from leaf |
| 723384004 | Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency (disorder) | y | descendant of concept mapped from leaf |
| 725136003 | Immunodeficiency by defective expression of human leukocyte antigen class 1 (disorder) | y | descendant of concept mapped from leaf |
| 24743004 | Complement deficiency disease (disorder) | y | descendant of concept mapped from leaf |
| 80255009 | Maternal transfer neutropenia (disorder) | y | descendant of concept mapped from leaf |
| 723385003 | Mendelian susceptibility to mycobacterial disease due to partial interferon regulatory factor 8 deficiency (disorder) | y | descendant of concept mapped from leaf |
| 40197009 | Chronic granulomatous disease, type IA (disorder) | y | descendant of concept mapped from leaf |
| 71610005 | Neutrophilic leukemoid reaction (disorder) | y | descendant of concept mapped from leaf |
| 49555001 | Severe combined immunodeficiency due to absent T cell receptor (disorder) | y | descendant of concept mapped from leaf |
| 116133005 | Congenital agammaglobulinemia (disorder) | y | descendant of concept mapped from leaf |
| 9893005 | Immunodeficiency with thymoma (disorder) | y | descendant of concept mapped from leaf |
| 234572005 | Benign combined immunodeficiency (disorder) | y | descendant of concept mapped from leaf |
| 398271008 | Predominantly T-cell defect (finding) | y | descendant of concept mapped from leaf |
| 721977007 | Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome (disorder) | y | descendant of concept mapped from leaf |
| 32092008 | Toxic neutropenia (disorder) | y | descendant of concept mapped from leaf |
| 65623009 | Immune neutropenia (disorder) | y | descendant of concept mapped from leaf |
| 234418001 | Chronic benign granulocytopenia (disorder) | y | descendant of concept mapped from leaf |
| 127067009 | Stress neutrophilia (disorder) | y | descendant of concept mapped from leaf |
| 234423001 | Chronic benign neutropenia (disorder) | y | descendant of concept mapped from leaf |
| 719827008 | X-linked immunoneurologic disorder (disorder) | y | descendant of concept mapped from leaf |
| 17182001 | Agranulocytosis (disorder) | y | descendant of concept mapped from leaf |
| 710927004 | Periodontitis co-occurrent with cyclical neutropenia (disorder) | y | descendant of concept mapped from leaf |
| 267538002 | Agranulocytopenic disorder (disorder) | n | via Query Table |
| 234537007 | Autosomal recessive hyperimmunoglobulin M syndrome (finding) | n | via Query Table |
| 938231000000103 | Mannan-binding protein deficiency | n | via Query Table |
| 660661000000101 | Polymorphonuclear neutrophil disorder NOS (disorder) | n | via Query Table |
| 693341000000104 | Predominantly T-cell immuno-deficiency NOS (finding) | n | via Query Table |
| 310589001 | Granulocytopenia (disorder) | n | via Query Table |
| 1050951000000106 | Immunoglobulin G4 deficiency | n | via Query Table |
| 906000 | AIDS with agranulocytosis (disorder) | n | via Query Table |
| 467901000000107 | [X]Immunodeficiency associated with major defect, unspecified | n | via Query Table |
| 192801000000104 | Schwachman's syndrome | n | via Query Table |
| 638281000000100 | Unspecified immunity deficiency (disorder) | n | via Query Table |
| 190984009 | Agammaglobulinemia NEC (finding) | n | via Query Table |
| 814211000000101 | Immune reconstitution syndrome (disorder) | n | via Query Table |
| 203592006 | X-linked severe combined immunodeficiency (disorder) | n | via Query Table |
| 72050006 | Agranulocytic angina (disorder) | n | via Query Table |
| 425229001 | Chemotherapy-induced neutropenia (disorder) | n | via Query Table |
| 191352003 | Congenital dysphagocytosis (disorder) | n | via Query Table |
| 646621000000103 | Combined immunity deficiency NOS (disorder) | n | via Query Table |
| 626051000000103 | Agranulocytosis NOS (disorder) | n | via Query Table |
| 69295006 | Cyclic neutropenia (disorder) | n | via Query Table |
| 757291000000109 | Hereditary C1 esterase inhibitor deficiency - deficient factor | n | via Query Table |
| 599441000000104 | Transient neonatal neutropenia NOS (disorder) | n | via Query Table |
| 656561000000105 | Congenital agranulocytosis NEC (disorder) | n | via Query Table |
| 192783000 | Schultz disease (disorder) | n | via Query Table |
| 411421000000102 | [X]Immunodeficiency associated with major defect, unspecified (disorder) | n | via Query Table |
| 236510007 | Lambda chain disease (disorder) | n | via Query Table |
| 83092002 | Shprintzen syndrome (disorder) | n | via Query Table |
| 609361000000103 | Deficiency of cell-mediated immunity NOS (finding) | n | via Query Table |
| 623081000000100 | Agammaglobulinemia NEC (finding) | n | via Query Table |
| 666921000000103 | Acquired neutropenia NEC (disorder) | n | via Query Table |
| 69624006 | Combined immunodeficiency disease in Arab foals (disorder) | n | via Query Table |
| 234536003 | X-linked hyperimmunoglobulin M syndrome (finding) | n | via Query Table |
| 191030000 | [X]Immunodeficiency associated with major defect, unspecified (disorder) | n | via Query Table |
| 41541007 | Hyperimmunoglobulin E syndrome (disorder) | n | via Query Table |
| 623061000000109 | Hypogammaglobulinemia NOS (finding) | n | via Query Table |
| 623071000000102 | Other selective immunoglobulin deficiency (finding) | n | via Query Table |
| 460436001 | 22q11 microdeletion with complete DiGeorge sequence (disorder) | n | via Query Table |
| 77128003 | DiGeorge sequence (disorder) | n | via Query Table |
| 832841000000103 | Immune reconstitution syndrome | n | via Query Table |
| 571321000000109 | Other specified agranulocytosis (disorder) | n | via Query Table |
| 62246005 | Acquired immunodeficiency syndrome-like syndrome (disorder) | n | via Query Table |
| 13263004 | Cyclic neutropenia in Gray Collie dogs (disorder) | n | via Query Table |
Codes not in the full codelist are in faint grey.