Permanent Immunosuppression (SNOMED) Draft



Coding system
SNOMED CT
Project
OpenSAFELY
Codelist ID
opensafely/permanent-immunosuppression-snomed
Version
2020-06-02-draft

Description

Automatically-generated equivalent of Permanent Immunosuppression

Methodology

See code on GitHub

References

  • ...

Signed off by

  • ...

This definition has been computed by taking the manually created full codelist and converting it to a list of rules that define the codelist.

Active Concepts
Inactive Concepts
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 in the definition are underlined. Codes in the full codelist are in blue. Related codes not in the codelist are in black.