[ { "phenotype_id": "PH3631", "phenotype_version_id": 8730, "name": "Permanent Immunosuppression (SNOMED)", "definition": "This codelist was taken from [OpenCodelists](https://www.opencodelists.org/), created by [OpenSAFELY](https://www.opensafely.org/). We recommend viewing this Phenotype on the OpenCodelist website to view the most recent version.\n\n\nAutomatically\\-generated equivalent of [Permanent Immunosuppression](/codelist/opensafely/permanent-immunosuppression/)\n\n\n© University of Oxford for the Bennett Institute for Applied Data Science 2025\\. This work may be copied freely for non\\-commercial research and study.\n\n", "implementation": null, "publications": null, "validation": null, "citation_requirements": null, "created": "2026-01-26T23:27:16.688403Z", "author": "OpenSAFELY", "collections": [ { "name": "OpenCodelist", "value": 31 }, { "name": "Phenotype Library", "value": 18 } ], "tags": null, "organisation": { "id": 1, "slug": "opensafely", "name": "OpenSAFELY" }, "world_access": 1, "updated": "2026-01-26T23:27:16.681365Z", "references": [], "signed_off": [], "methodology": "See [code on GitHub](https://github.com/opensafely-core/opencodelists/blob/248fe3397327e019a2d93830bd5fdb1c2562b23d/codelists/management/commands/convert_codelist.py)\n\n", "coding_system": [ { "name": "SNOMED CT codes", "value": 9 } ], "open_codelist_id": "opensafely/permanent-immunosuppression-snomed", "source_reference": "https://www.opencodelists.org/codelist/opensafely/permanent-immunosuppression-snomed/2020-06-02", "concept_information": [ { "concept_id": 8907, "concept_version_id": 16392, "concept_name": "opensafely/permanent-immunosuppression-snomed/2020-06-02", "coding_system": { "id": 9, "name": "SNOMED CT codes", "description": "SNOMED CT codes" }, "phenotype_id": "PH3631", "phenotype_version_id": 8730, "phenotype_name": "Permanent Immunosuppression (SNOMED)", "code_attribute_header": [ "active", "notes" ], "codes": [ { "code": "103077004", "description": "Immunodeficiency secondary to neoplasm (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "103078009", "description": "Immunodeficiency secondary to trauma (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "103079001", "description": "Immunodeficiency caused by corticosteroid (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "103080003", "description": "Immunodeficiency secondary to radiation therapy (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "103081004", "description": "Immunodeficiency secondary to chemotherapy (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "1050951000000106", "description": "Immunoglobulin G4 deficiency", "attributes": { "active": "n", "notes": "via Query Table" } }, { "code": "105601003", "description": "Quantitative disorder of neutrophils (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "105602005", "description": "Quantitative abnormality of granulocytes (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "10746341000119109", "description": "Acquired immune deficiency syndrome complicating childbirth (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "10838971000119103", "description": "Immunodeficiency caused by long term therapeutic use of drug (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "111396008", "description": "Chédiak-Higashi syndrome (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "111584000", "description": "Reticular dysgenesis (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "111585004", "description": "Neutropenia associated with autoimmune disease (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "111587007", "description": "Severe combined immunodeficiency due to absent interleukin-2 receptor (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "116133005", "description": "Congenital agammaglobulinemia (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "119249001", "description": "Agammaglobulinemia (finding)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "12631000119106", "description": "Immunoglobulin G deficiency (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "127067009", "description": "Stress neutrophilia (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "129639005", "description": "Hereditary neutrophilia (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "129640007", "description": "Benign granulocytopenia in childhood (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "129641006", "description": "Chronic benign neutropenia of childhood (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "129642004", "description": "Chronic idiopathic immunoneutropenia in adults (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "129643009", "description": "Chronic hypoplastic neutropenia (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "13263004", "description": "Cyclic neutropenia in Gray Collie dogs (disorder)", "attributes": { "active": "n", "notes": "via Query Table" } }, { "code": "14333004", "description": "Alloimmune neonatal neutropenia (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "17182001", "description": "Agranulocytosis (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "183023001", "description": "Transplant immunosuppression (procedure)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "18827005", "description": "Complement abnormality (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "190979003", "description": "Selective immunoglobulin A deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "190980000", "description": "Selective immunoglobulin M deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "190981001", "description": "Selective immunoglobulin G deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "190984009", "description": "Agammaglobulinemia NEC (finding)", "attributes": { "active": "n", "notes": "via Query Table" } }, { "code": "190993005", "description": "Autosomal recessive severe combined immunodeficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "190995003", "description": "Thymic aplasia or dysplasia with immunodeficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "190996002", "description": "Severe combined immunodeficiency with reticular dysgenesis (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "190997006", "description": "Severe combined immunodeficiency with low T- and B-cell numbers (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "190998001", "description": "Severe combined immunodeficiency with low or normal B-cell numbers (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "191001007", "description": "Major histocompatibility complex class I deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "191002000", "description": "Major histocompatibility complex class II deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "191008001", "description": "Immunodeficiency following hereditary defective response to Epstein-Barr virus (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "191011000", "description": "Common variable immunodeficiency with predominant abnormalities of B-cell numbers and functions (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "191012007", "description": "Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "191013002", "description": "Common variable immunodeficiency with autoantibodies to B- or T-cells (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "191018006", "description": "Lymphocyte function antigen-1 defect (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "191030000", "description": "[X]Immunodeficiency associated with major defect, unspecified (disorder)", "attributes": { "active": "n", "notes": "via Query Table" } }, { "code": "191338000", "description": "Primary splenic neutropenia (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "191347008", "description": "Cyclical neutropenia (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "191352003", "description": "Congenital dysphagocytosis (disorder)", "attributes": { "active": "n", "notes": "via Query Table" } }, { "code": "192783000", "description": "Schultz disease (disorder)", "attributes": { "active": "n", "notes": "via Query Table" } }, { "code": "192801000000104", "description": "Schwachman's syndrome", "attributes": { "active": "n", "notes": "via Query Table" } }, { "code": "203592006", "description": "X-linked severe combined immunodeficiency (disorder)", "attributes": { "active": "n", "notes": "via Query Table" } }, { "code": "21527007", "description": "Chronic granulomatous disease, type IV (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "22406001", "description": "Severe combined immunodeficiency due to absent lymphoid stem cells (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "23238000", "description": "Common variable agammaglobulinemia (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234367000", "description": "Pancytopenia with pancreatitis (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234416002", "description": "X-linked hypogammaglobulinemia (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234418001", "description": "Chronic benign granulocytopenia (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "234423001", "description": "Chronic benign neutropenia (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "234424007", "description": "Metabolic neutropenia (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234425008", "description": "Autoimmune neutropenia (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234426009", "description": "Corticosteroid-induced neutrophilia (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "234430007", "description": "CR3-receptor deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234431006", "description": "Specific granule deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234433009", "description": "Myeloperoxidase deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234434003", "description": "Alders syndrome (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234435002", "description": "Hereditary hypersegmentation (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234436001", "description": "Hemolytic erythrophagocytic syndrome (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "234437005", "description": "Hemophagocytic lymphohistiocytosis (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "234484005", "description": "May-Hegglin anomaly (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234532001", "description": "Immunodeficiency disorder (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234533006", "description": "X-linked agammaglobulinemia with growth hormone deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234534000", "description": "Autosomal agammaglobulinemia with absent B-cells (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234535004", "description": "Selective immunoglobulin dysfunction (finding)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234536003", "description": "X-linked hyperimmunoglobulin M syndrome (finding)", "attributes": { "active": "n", "notes": "via Query Table" } }, { "code": "234537007", "description": "Autosomal recessive hyperimmunoglobulin M syndrome (finding)", "attributes": { "active": "n", "notes": "via Query Table" } }, { "code": "234538002", "description": "Hyperimmunoglobulin D with periodic fever (finding)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234539005", "description": "Immunoglobulin heavy chain deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234540007", "description": "Selective immunoglobulin E deficiency (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "234541006", "description": "Selective immunoglobulin D deficiency (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "234542004", "description": "Selective immunoglobulin M and immunoglobulin A deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234543009", "description": "Immunoglobulin light chain deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234544003", "description": "Immunoglobulin subclass deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234546001", "description": "Immunoglobulin G2 deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234547005", "description": "Combined immunoglobulin G2 and G4 deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234548000", "description": "Immunoglobulin G3 deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234549008", "description": "Immunoglobulin G4 deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234550008", "description": "Immunoglobulin G1 deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234551007", "description": "Immunoglobulin A1 deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234552000", "description": "Immunoglobulin A2 deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234553005", "description": "Immunoglobulin-associated molecule deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234554004", "description": "Secretory piece deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234555003", "description": "Defective immunoglobulin glycosylation (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234556002", "description": "Specific antibody deficiency (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "234557006", "description": "Anti-polysaccharide antibody deficiency (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "234558001", "description": "Anti-haemophilus influenzae B polysaccharide antibody deficiency (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "234559009", "description": "Anti-pneumococcal polysaccharide antibody deficiency (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "234560004", "description": "Anti-meningococcal polysaccharide A antibody deficiency (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "234561000", "description": "Anti-meningococcal polysaccharide C antibody deficiency (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "234562007", "description": "Anti-protein antibody deficiency (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "234563002", "description": "Anti-staphylococcal antibody deficiency (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "234564008", "description": "Primary immunoglobulin catabolism abnormality (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "234565009", "description": "Immunoglobulin hypercatabolism (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "234566005", "description": "Familial immunoglobulin hypercatabolism (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "234568006", "description": "Chronic mucocutaneous candidiasis (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234570002", "description": "Severe combined immunodeficiency with maternofetal engraftment (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234571003", "description": "Warts, hypogammaglobulinemia, infections, and myelokathexis (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234572005", "description": "Benign combined immunodeficiency (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "234573000", "description": "Phagocytic cell defect (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "234574006", "description": "Disorder of phagocytic cell number (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } }, { "code": "234576008", "description": "Chronic familial neutropenia (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234577004", "description": "Lipochrome histiocytosis - familial (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234578009", "description": "Defective phagocytic cell opsonization (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234579001", "description": "Mannan-binding protein deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234580003", "description": "Defective phagocytic cell chemotaxis (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234581004", "description": "Defective phagocytic cell adhesion (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234582006", "description": "Leukocyte adhesion deficiency - type 1 (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234583001", "description": "Leukocyte adhesion deficiency - type 2 (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234584007", "description": "Tuftsin deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234585008", "description": "Defective phagocytic cell killing (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234586009", "description": "Leukocyte glucose-6-phosphate dehydrogenase deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234587000", "description": "Neutrophil lactoferrin deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234588005", "description": "Neutrophil secondary granule deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234589002", "description": "Glutathione synthetase deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234590006", "description": "Gluthathione peroxidase deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234591005", "description": "Combined phagocytic defect (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234593008", "description": "Classical complement pathway abnormality (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234594002", "description": "Complement 1q deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234595001", "description": "Complement 1q beta chain deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234596000", "description": "Complement 1q dysfunction (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234597009", "description": "Complement 1r deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234598004", "description": "Complement 1s deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234599007", "description": "Complement 2 deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234600005", "description": "Complement 4 deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234601009", "description": "Complement 4A deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234602002", "description": "Complement 4B deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234603007", "description": "Complement 3 deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234604001", "description": "Alternative pathway deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234605000", "description": "Factor B deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234607008", "description": "Factor D deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234608003", "description": "Terminal component deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234609006", "description": "Complement 5 deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234611002", "description": "Complement 6 deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234612009", "description": "Complement 7 deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234613004", "description": "Combined complement 6 and 7 deficiencies (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234614005", "description": "Complement 8 beta chain deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234615006", "description": "Complement 8 beta chain dysfunction (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234616007", "description": "Complement 8 alpha-gamma deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234617003", "description": "Complement 9 deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234618008", "description": "Complement regulatory factor defect (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234619000", "description": "Hereditary C1 esterase inhibitor deficiency - deficient factor (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234620006", "description": "Hereditary C1 esterase inhibitor deficiency - dysfunctional factor (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234621005", "description": "Factor I deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234622003", "description": "Factor H deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234623008", "description": "Complement 4 binding protein deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234624002", "description": "Decay accelerating factor deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234625001", "description": "Homologous restriction factor deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234626000", "description": "Complement 5a inhibitor deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234627009", "description": "Anaphylotoxin inactivator deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234628004", "description": "Complement receptor deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234629007", "description": "Complement receptor 1 deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234630002", "description": "Complement receptor 3 deficiency (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "234631003", "description": 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"code": "906000", "description": "AIDS with agranulocytosis (disorder)", "attributes": { "active": "n", "notes": "via Query Table" } }, { "code": "91918005", "description": "Congenital absence of thymus (disorder)", "attributes": { "active": "y", "notes": "direct mapping" } }, { "code": "938231000000103", "description": "Mannan-binding protein deficiency", "attributes": { "active": "n", "notes": "via Query Table" } }, { "code": "9893005", "description": "Immunodeficiency with thymoma (disorder)", "attributes": { "active": "y", "notes": "descendant of concept mapped from leaf" } } ] } ], "coding_system_release": "", "open_codelist_version_id": "55914b31", "open_codelist_version_tag": "2020-06-02", "status": 1, "doi": "https://doi.org/10.48533/9ajg-7n42", "is_deleted": false, "publish_status": 2, "owner": "ieuan.scanlon", "template": { "id": 3, "name": "OpenCodelists Phenotype", "description": "OpenSafely's OpenCodelist Phenotype, visit https://www.opencodelists.org/ to learn more", "version_id": 1 }, "versions": [ { "version_id": 8730, "version_name": "Permanent Immunosuppression (SNOMED)", "version_date": "2026-01-26T23:27:16.699665Z", "is_published": true, "is_latest": true } ] } ]