Permanent Immunosuppression
Codelist metadata
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Coding system
- CTV3 (Read V3)
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Coding system release
- unknown
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Organisation
- OpenSAFELY
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Codelist ID
- opensafely/permanent-immunosuppression
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Version Tag
- 2020-06-02
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Version ID
- 268d3303
Versions
About
Description
Codes indicating a diagnosis of a permanent immunosuppression excluding HIV, and including genetic causes of immunosuppression
Methodology
TODO
References
Signed off by
- Liam Smeeth, (April 24, 2020)
- Helen McDonald, (April 23, 2020)
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.
| CTV3ID | CTV3PreferredTermDesc |
|---|---|
| C390y | Other specified deficiency of humoral immunity |
| C390z | Deficiency of humoral immunity NOS |
| C391. | Deficiencies of cell-mediated immunity |
| C391z | Deficiency of cell-mediated immunity NOS |
| C393. | Unspecified immunity deficiency |
| Cyu00 | [X]Other immunodeficiencies+predominantly antibody defects |
| Cyu05 | [X]Other specified immunodeficiency disorders |
| D401z | Polymorphonuclear neutrophil disorder NOS |
| X20GZ | Immunodeficiency disorder |
| X20HE | T-lymphocyte deficiency |
| XaYgn | Immune reconstitution syndrome |
| XE11u | Deficiencies of humoral immunity |
| XE11w | Predominantly T-cell immuno-deficiency NOS |
| C30yy | (Adenosine deamin def) or (oth sp disturb amino acid metab) |
| C3760 | C1 esterase inhibitor deficiency |
| C390. | (Deficiencies of humoral immunity) or (agammaglobulinaemia) |
| C3901 | Selective immunoglobulin A deficiency |
| C3902 | Selective immunoglobulin M deficiency |
| C3903 | Selective immunoglobulin G deficiency |
| C3904 | Other selective immunoglobulin deficiency |
| C3905 | Hypogammaglob:[cong][agammaglob:(Brut)(cong sex-link & [X])] |
| C3906 | Hyperimmunoglobulin M syndrome |
| C3907 | Common variable immunodeficiency |
| C3909 | Agammaglobulinaemia NEC |
| C390A | Dysimmunoglobulinaemia NEC |
| C3910 | Cellular immunity syndr (& T-lymphocyte deficiency [& NOS]) |
| C3911 | DiGeorge syndrome |
| C3912 | Wiskott-Aldrich syndrome |
| C3913 | Nezelof's syndrome |
| C392. | Combined T-cell and B-cell immunodeficiency |
| C3920 | Autosomal recessive severe combined immunodeficiency |
| C3921 | (Severe combined immunodefic) or (Swiss agammaglobulinaemia) |
| C3922 | Thymic aplasia or dysplasia with immunodeficiency |
| C3923 | Severe combined immunodefiency with reticular dysgenesis |
| C3924 | Severe combined immunodef with low T- and B-cell numbers |
| C3925 | Severe combined immunodef with low or normal B-cell numbers |
| C3928 | Major histocompatibility complex class I deficiency |
| C3929 | Major histocompatibility complex class II deficiency |
| C392z | Combined immunity deficiency NOS |
| C396. | Immunodef follow hereditary defect respon Epstein-Barr vir |
| C3980 | Com var immunodef with predom abn B-cell numbers and functns |
| C3981 | Common var immunodef predom immunoregulatory T-cell disorder |
| C3982 | Common variable immunodef wth autoantibod to B- or T-cells |
| C39y0 | Lymphocyte function antigen-1 defect |
| Cyu01 | [X]Other combined immunodeficiency disorders |
| Cyu02 | [X]Immunodeficiency associatd+other specified major defects |
| Cyu03 | [X]Immunodeficiency associated+major defect, unspecified |
| Cyu04 | [X]Other common variable immunodeficiencies |
| D2016 | Pancytopenia: [with malformation]/[with pancreatitis]/[NOS] |
| D4001 | Primary splenic neutropenia |
| D4005 | Congenital: [neutropenia] or [agranulocytosis NEC] |
| D4009 | Cyclical neutropenia |
| D401. | (Funct dis polymorph neutroph)(Job's)(fam lipochr histiocyt) |
| D4010 | Congenital dysphagocytosis |
| D402. | (Anomaly: [genet leucocyt][epon vars]) or (Ched-Higash synd) |
| F14y0 | Ataxia telangiectasia |
| M15y3 | Complement 5 dysfunction |
| X20CO | Pancytopenia with pancreatitis |
| X20Da | Congenital agranulocytosis NEC |
| X20Db | X-linked hypogammaglobulinaemia |
| X20De | Chronic idiopathic neutropenia |
| X20Df | Severe congenital neutropenia |
| X20Dk | Myelokathexis |
| X20Dl | Metabolic neutropenia |
| X20Dn | Autoimmune neutropenia |
| X20Dv | Chediak-Higashi syndrome |
| X20Dw | Hyperimmunoglobulin E syndrome |
| X20Dx | CR3-receptor deficiency |
| X20Dy | Specific granule deficiency |
| X20E0 | Chronic granulomatous disease |
| X20E1 | Myeloperoxidase deficiency |
| X20E4 | Hereditary hypersegmentation |
| X20Ga | Primary immunodeficiency |
| X20Gb | Agammaglobulinaemia |
| X20Gc | X-linked agammaglobulinaemia |
| X20Gd | X-linked agammaglobulinaemia with growth hormone deficiency |
| X20Ge | Autosomal agammaglobulinaemia with absent B-cells |
| X20Gf | Selective immunoglobulin dysfunction |
| X20Gg | X-linked hyperimmunoglobulin M syndrome |
| X20Gh | Autosomal recessive hyperimmunoglobulin M syndrome |
| X20Gj | Hyperimmunoglobulin D with periodic fever |
| X20Gk | Immunoglobulin heavy chain deficiency |
| X20Gn | Selective immunoglobulin M and immunoglobulin A deficiency |
| X20Go | Immunoglobulin light chain deficiency |
| X20Gp | Kappa light chain deficiency |
| X20Gq | Lambda light chain deficiency |
| X20Gr | Immunoglobulin subclass deficiency |
| X20Gt | Immunoglobulin G2 deficiency |
| X20Gu | Combined immunoglobulin G2 and G4 deficiency |
| X20Gv | Immunoglobulin G3 deficiency |
| X20Gw | Immunoglobulin G4 deficiency |
| X20Gx | Immunoglobulin G1 deficiency |
| X20Gy | Immunoglobulin A1 deficiency |
| X20Gz | Immunoglobulin A2 deficiency |
| X20H0 | Immunoglobulin-associated molecule deficiency |
| X20H1 | Secretory piece deficiency |
| X20H2 | Defective immunoglobulin glycosylation |
| X20Ha | Schwachman's syndrome |
| X20Hb | Defective phagocytic cell adhesion |
| X20Hc | Leucocyte adhesion deficiency - type 1 |
| X20Hd | Leucocyte adhesion deficiency - type 2 |
| X20Hf | Tuftsin deficiency |
| X20HF | Chronic mucocutaneous candidiasis |
| X20Hg | Defective phagocytic cell killing |
| X20HH | Combined immunodeficiency with maturation pathway defect |
| X20HI | Reticular dysgenesis |
| X20Hi | Leucocyte glucose-6-phosphate dehydrogenase deficiency |
| X20HJ | X-linked severe combined immunodeficiency |
| X20HK | Severe combined immunodeficiency with short-limbed dwarfism |
| X20Hk | Neutrophil lactoferrin deficiency |
| X20HL | Bare lymphocyte syndrome |
| X20Hl | Neutrophil secondary granule deficiency |
| X20HM | Familial erythrophagocytic lymphohistiocytosis |
| X20Hm | Gluthathione synthetase deficiency |
| X20HN | Severe comb immunodeficiency with maternofetal engraftment |
| X20Hn | Gluthathione peroxidase deficiency |
| X20HO | Warts, hypogammaglobulinaemia, infections, and myelokathexis |
| X20Hp | Combined phagocytic defect |
| X20Ht | Classical complement pathway abnormality |
| X20HU | Chronic familial neutropaenia |
| X20Hu | Complement 1q deficiency |
| X20HV | Lipochrome histiocytosis - familial |
| X20Hv | Complement 1q beta chain deficiency |
| X20HW | Defective phagocytic cell opsonisation |
| X20Hw | Complement 1q dysfunction |
| X20HX | Mannan-binding protein deficiency |
| X20Hx | Complement 1r deficiency |
| X20HY | Defective phagocytic cell chemotaxis |
| X20Hy | Complement 1s deficiency |
| X20HZ | Lazy leucocyte syndrome |
| X20Hz | Complement 2 deficiency |
| X20I0 | Complement 4 deficiency |
| X20I1 | Complement 4A deficiency |
| X20I2 | Complement 4B deficiency |
| X20I3 | Complement 3 deficiency |
| X20I4 | Alternative pathway deficiency |
| X20I5 | Properdin deficiency |
| X20I6 | Factor B deficiency |
| X20I7 | Factor D deficiency |
| X20I8 | Terminal component deficiency |
| X20I9 | Complement 5 deficiency |
| X20Ia | Chromosome 18 syndromes and antibody deficiency |
| X20IB | Complement 6 deficiency |
| X20Ib | Chromosome 22 abnormalities with hypogammaglobulinaemia |
| X20IC | Complement 7 deficiency |
| X20Ic | Monosomy 22 and absence of immunoglobulin A |
| X20ID | Combined complement 6 and 7 deficiencies |
| X20Id | Deletion of X-chromosome and hypogammaglobulinaemia |
| X20IE | Complement 8 beta chain deficiency |
| X20Ie | Microcephaly, normal intelligence and immunodeficiency |
| X20IF | Complement 8 beta chain dysfunction |
| X20If | Triple X syndrome, epilepsy, and hypogammaglobulinaemia |
| X20IG | Complement 8 alpha-gamma deficiency |
| X20Ig | 18-p syndrome with associated immunodeficiency |
| X20IH | Complement 9 deficiency |
| X20Ih | Immunodeficiency with multiple organ system abnormalities |
| X20II | Complement regulatory factor defect |
| X20IJ | Hereditary C1 esterase inhibitor defic - deficient factor |
| X20Ij | Partial albinism with immunodeficiency |
| X20IK | Hereditary C1 esterase inhib defic - dysfunctional factor |
| X20Ik | X-linked lymphoproliferative syndrome |
| X20IL | Factor I deficiency |
| X20IM | Factor H deficiency |
| X20IN | Complement 4 binding protein deficiency |
| X20IO | Decay accelerating factor deficiency |
| X20IP | Homologous restriction factor deficiency |
| X20IQ | Complement 5a inhibitor deficiency |
| X20IR | Anaphylotoxin inactivator deficiency |
| X20IS | Complement receptor deficiency |
| X20IT | Complement receptor 1 deficiency |
| X20IU | Complement receptor 3 deficiency |
| X20IV | Immunodeficiency with major anomalies |
| X20IW | Immunodeficiency associated with chromosomal abnormality |
| X20IY | Bloom syndrome |
| X20IZ | Centromeric instability of chromosomes 1,9+16 + immunodefic |
| X20RX | Familial chronic mucocutaneous candidiasis |
| X40Ua | Adenosine deaminase deficiency |
| X40Uc | Purine nucleoside phosphorylase deficiency |
| X70Qz | Familial chronic mucocutaneous candidiasis - late onset type |
| X70R0 | Chronic localised mucocutaneous candidiasis |
| X70R1 | Chronic diffuse mucocutaneous candidiasis |
| X789w | Immuno-osseous dysplasia |
| Xa9Az | Phagocytic cell dysfunction |
| XaA0r | Metaphys chondrodysplas, McKusick type with assoc immunodef |
| XE11v | Congenital hypogammaglobulinaemia |
| XE13a | Agammaglobulinaemia &/or hypo-gammaglobulinaemia |
| XE14B | Chronic idiopathic neutropaenia |
| XE14F | Congenital neutropenia |
| XE14H | Functional disorders of polymorphonuclear neutrophils |
| 8C31. | Transplant immunosuppression |
| PK281 | Congenital absence of thymus |
Codes not in the full codelist are in faint grey.