{
  "concept_id": 4154,
  "concept_version_id": 11514,
  "coding_system": {
    "id": 9,
    "name": "SNOMED  CT codes",
    "description": "SNOMED CT codes"
  },
  "name": "Immunological (SNOMED-CT)",
  "description": null,
  "author": "",
  "entry_date": "2025-01-19",
  "validation_performed": false,
  "validation_description": null,
  "publication_doi": "",
  "publication_link": "",
  "secondary_publication_links": null,
  "paper_published": false,
  "source_reference": "",
  "citation_requirements": null,
  "owner_access": 3,
  "group_access": 1,
  "world_access": 1,
  "tags": null,
  "collections": null,
  "created_by": null,
  "modified_by": null,
  "owner": null,
  "group": null,
  "phenotype_owner": "PH1706",
  "phenotype_owner_history_id": 3631,
  "requested_entity_id": null,
  "components": [
    {
      "id": 9981,
      "name": "Inclusion 1",
      "logical_type": "INCLUDE",
      "source_type": "FILE_IMPORT",
      "source": "text/csv",
      "codes": [
        {
          "id": 534906,
          "code": "103075007",
          "description": "Humoral immune defect (finding)"
        },
        {
          "id": 534907,
          "code": "103077004",
          "description": "Immunodeficiency secondary to neoplasm (disorder)"
        },
        {
          "id": 534908,
          "code": "103078009",
          "description": "Immunodeficiency secondary to trauma (disorder)"
        },
        {
          "id": 534909,
          "code": "103079001",
          "description": "Immunodeficiency caused by corticosteroid (disorder)"
        },
        {
          "id": 534910,
          "code": "103080003",
          "description": "Immunodeficiency secondary to radiation therapy (disorder)"
        },
        {
          "id": 534911,
          "code": "103081004",
          "description": "Immunodeficiency secondary to chemotherapy (disorder)"
        },
        {
          "id": 534912,
          "code": "111587007",
          "description": "Severe combined immunodeficiency due to absent interleukin-2 receptor (disorder)"
        },
        {
          "id": 534913,
          "code": "116133005",
          "description": "Congenital agammaglobulinemia (disorder)"
        },
        {
          "id": 534914,
          "code": "119249001",
          "description": "Agammaglobulinemia (finding)"
        },
        {
          "id": 534915,
          "code": "119250001",
          "description": "Hypogammaglobulinemia (finding)"
        },
        {
          "id": 534916,
          "code": "123785006",
          "description": "Immunoglobulin G subclass deficiency (finding)"
        },
        {
          "id": 534917,
          "code": "124274002",
          "description": "Deficiency of adenine phosphoribosyltransferase (disorder)"
        },
        {
          "id": 534918,
          "code": "124281009",
          "description": "Deficiency of dimethylallyltranstransferase (disorder)"
        },
        {
          "id": 534919,
          "code": "124450003",
          "description": "Deficiency of deoxyribonuclease I (disorder)"
        },
        {
          "id": 534920,
          "code": "124517001",
          "description": "Deficiency of allantoinase (disorder)"
        },
        {
          "id": 534921,
          "code": "124521008",
          "description": "Deficiency of adenine deaminase (disorder)"
        },
        {
          "id": 534922,
          "code": "124703008",
          "description": "Deficiency of cholate-CoA ligase (disorder)"
        },
        {
          "id": 534923,
          "code": "124950009",
          "description": "Deficiency of immunoglobulin (disorder)"
        },
        {
          "id": 534924,
          "code": "12631000119106",
          "description": "Immunoglobulin G deficiency (disorder)"
        },
        {
          "id": 534925,
          "code": "12814002",
          "description": "B lymphocyte disorder (disorder)"
        },
        {
          "id": 534926,
          "code": "129644003",
          "description": "Myeloperoxidase deficiency syndrome (disorder)"
        },
        {
          "id": 534927,
          "code": "15012007",
          "description": "Granulocyte abnormality due to immune defect (disorder)"
        },
        {
          "id": 534928,
          "code": "16318001000119107",
          "description": "Hypogammaglobulinemia due to multiple myeloma (disorder)"
        },
        {
          "id": 534929,
          "code": "18827005",
          "description": "Complement abnormality (disorder)"
        },
        {
          "id": 534930,
          "code": "190979003",
          "description": "Selective immunoglobulin A deficiency (disorder)"
        },
        {
          "id": 534931,
          "code": "190980000",
          "description": "Selective immunoglobulin M deficiency (disorder)"
        },
        {
          "id": 534932,
          "code": "190981001",
          "description": "Selective immunoglobulin G deficiency (disorder)"
        },
        {
          "id": 534933,
          "code": "190993005",
          "description": "Autosomal recessive severe combined immunodeficiency (disorder)"
        },
        {
          "id": 534934,
          "code": "190995003",
          "description": "Thymic aplasia or dysplasia with immunodeficiency (disorder)"
        },
        {
          "id": 534935,
          "code": "190996002",
          "description": "Severe combined immunodeficiency with reticular dysgenesis (disorder)"
        },
        {
          "id": 534936,
          "code": "190997006",
          "description": "Severe combined immunodeficiency with low T- and B-cell numbers (disorder)"
        },
        {
          "id": 534937,
          "code": "190998001",
          "description": "Severe combined immunodeficiency with low or normal B-cell numbers (disorder)"
        },
        {
          "id": 534938,
          "code": "191001007",
          "description": "Major histocompatibility complex class I deficiency (disorder)"
        },
        {
          "id": 534939,
          "code": "191002000",
          "description": "Major histocompatibility complex class II deficiency (disorder)"
        },
        {
          "id": 534940,
          "code": "191008001",
          "description": "Immunodeficiency following hereditary defective response to Epstein-Barr virus (disorder)"
        },
        {
          "id": 534941,
          "code": "191011000",
          "description": "Common variable immunodeficiency with predominant abnormalities of B-cell numbers and functions (disorder)"
        },
        {
          "id": 534942,
          "code": "191012007",
          "description": "Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder)"
        },
        {
          "id": 534943,
          "code": "191013002",
          "description": "Common variable immunodeficiency with autoantibodies to B- or T-cells (disorder)"
        },
        {
          "id": 534944,
          "code": "191018006",
          "description": "Lymphocyte function antigen-1 defect (disorder)"
        },
        {
          "id": 534945,
          "code": "21043008",
          "description": "Neutrophil cytomatrix disorder (disorder)"
        },
        {
          "id": 534946,
          "code": "21527007",
          "description": "Chronic granulomatous disease, type IV (disorder)"
        },
        {
          "id": 534947,
          "code": "22406001",
          "description": "Severe combined immunodeficiency due to absent lymphoid stem cells (disorder)"
        },
        {
          "id": 534948,
          "code": "23132008",
          "description": "Amyloid light-chain amyloidosis (disorder)"
        },
        {
          "id": 534949,
          "code": "23238000",
          "description": "Common variable agammaglobulinemia (disorder)"
        },
        {
          "id": 534950,
          "code": "234403002",
          "description": "Phosphoglycerokinase deficiency (disorder)"
        },
        {
          "id": 534951,
          "code": "234416002",
          "description": "X-linked hypogammaglobulinemia (disorder)"
        },
        {
          "id": 534952,
          "code": "234429002",
          "description": "Chemotactic disorder (disorder)"
        },
        {
          "id": 534953,
          "code": "234430007",
          "description": "CR3-receptor deficiency (disorder)"
        },
        {
          "id": 534954,
          "code": "234431006",
          "description": "Specific granule deficiency (disorder)"
        },
        {
          "id": 534955,
          "code": "234433009",
          "description": "Myeloperoxidase deficiency (disorder)"
        },
        {
          "id": 534956,
          "code": "234532001",
          "description": "Immunodeficiency disorder (disorder)"
        },
        {
          "id": 534957,
          "code": "234533006",
          "description": "X-linked agammaglobulinemia with growth hormone deficiency (disorder)"
        },
        {
          "id": 534958,
          "code": "234534000",
          "description": "Autosomal agammaglobulinemia with absent B-cells (disorder)"
        },
        {
          "id": 534959,
          "code": "234538002",
          "description": "Hyperimmunoglobulin D with periodic fever (finding)"
        },
        {
          "id": 534960,
          "code": "234539005",
          "description": "Immunoglobulin heavy chain deficiency (disorder)"
        },
        {
          "id": 534961,
          "code": "234540007",
          "description": "Selective immunoglobulin E deficiency (disorder)"
        },
        {
          "id": 534962,
          "code": "234541006",
          "description": "Selective immunoglobulin D deficiency (disorder)"
        },
        {
          "id": 534963,
          "code": "234542004",
          "description": "Selective immunoglobulin M and immunoglobulin A deficiency (disorder)"
        },
        {
          "id": 534964,
          "code": "234543009",
          "description": "Immunoglobulin light chain deficiency (disorder)"
        },
        {
          "id": 534965,
          "code": "234544003",
          "description": "Immunoglobulin subclass deficiency (disorder)"
        },
        {
          "id": 534966,
          "code": "234546001",
          "description": "Immunoglobulin G2 deficiency (disorder)"
        },
        {
          "id": 534967,
          "code": "234547005",
          "description": "Combined immunoglobulin G2 and G4 deficiency (disorder)"
        },
        {
          "id": 534968,
          "code": "234548000",
          "description": "Immunoglobulin G3 deficiency (disorder)"
        },
        {
          "id": 534969,
          "code": "234549008",
          "description": "Immunoglobulin G4 deficiency (disorder)"
        },
        {
          "id": 534970,
          "code": "234550008",
          "description": "Immunoglobulin G1 deficiency (disorder)"
        },
        {
          "id": 534971,
          "code": "234551007",
          "description": "Immunoglobulin A1 deficiency (disorder)"
        },
        {
          "id": 534972,
          "code": "234552000",
          "description": "Immunoglobulin A2 deficiency (disorder)"
        },
        {
          "id": 534973,
          "code": "234553005",
          "description": "Immunoglobulin-associated molecule deficiency (disorder)"
        },
        {
          "id": 534974,
          "code": "234554004",
          "description": "Secretory piece deficiency (disorder)"
        },
        {
          "id": 534975,
          "code": "234555003",
          "description": "Defective immunoglobulin glycosylation (disorder)"
        },
        {
          "id": 534976,
          "code": "234556002",
          "description": "Specific antibody deficiency (disorder)"
        },
        {
          "id": 534977,
          "code": "234557006",
          "description": "Anti-polysaccharide antibody deficiency (disorder)"
        },
        {
          "id": 534978,
          "code": "234558001",
          "description": "Anti-haemophilus influenzae B polysaccharide antibody deficiency (disorder)"
        },
        {
          "id": 534979,
          "code": "234559009",
          "description": "Anti-pneumococcal polysaccharide antibody deficiency (disorder)"
        },
        {
          "id": 534980,
          "code": "234560004",
          "description": "Anti-meningococcal polysaccharide A antibody deficiency (disorder)"
        },
        {
          "id": 534981,
          "code": "234561000",
          "description": "Anti-meningococcal polysaccharide C antibody deficiency (disorder)"
        },
        {
          "id": 534982,
          "code": "234562007",
          "description": "Anti-protein antibody deficiency (disorder)"
        },
        {
          "id": 534983,
          "code": "234563002",
          "description": "Anti-staphylococcal antibody deficiency (disorder)"
        },
        {
          "id": 534984,
          "code": "234570002",
          "description": "Severe combined immunodeficiency with maternofetal engraftment (disorder)"
        },
        {
          "id": 534985,
          "code": "234571003",
          "description": "Warts, hypogammaglobulinemia, infections, and myelokathexis (disorder)"
        },
        {
          "id": 534986,
          "code": "234572005",
          "description": "Benign combined immunodeficiency (disorder)"
        },
        {
          "id": 534987,
          "code": "234573000",
          "description": "Phagocytic cell defect (disorder)"
        },
        {
          "id": 534988,
          "code": "234578009",
          "description": "Defective phagocytic cell opsonization (disorder)"
        },
        {
          "id": 534989,
          "code": "234579001",
          "description": "Mannan-binding protein deficiency (disorder)"
        },
        {
          "id": 534990,
          "code": "234580003",
          "description": "Defective phagocytic cell chemotaxis (disorder)"
        },
        {
          "id": 534991,
          "code": "234582006",
          "description": "Leukocyte adhesion deficiency - type 1 (disorder)"
        },
        {
          "id": 534992,
          "code": "234583001",
          "description": "Leukocyte adhesion deficiency - type 2 (disorder)"
        },
        {
          "id": 534993,
          "code": "234585008",
          "description": "Defective phagocytic cell killing (disorder)"
        },
        {
          "id": 534994,
          "code": "234586009",
          "description": "Leukocyte glucose-6-phosphate dehydrogenase deficiency (disorder)"
        },
        {
          "id": 534995,
          "code": "234587000",
          "description": "Neutrophil lactoferrin deficiency (disorder)"
        },
        {
          "id": 534996,
          "code": "234588005",
          "description": "Neutrophil secondary granule deficiency (disorder)"
        },
        {
          "id": 534997,
          "code": "234593008",
          "description": "Classical complement pathway abnormality (disorder)"
        },
        {
          "id": 534998,
          "code": "234594002",
          "description": "Complement 1q deficiency (disorder)"
        },
        {
          "id": 534999,
          "code": "234595001",
          "description": "Complement 1q beta chain deficiency (disorder)"
        },
        {
          "id": 535000,
          "code": "234596000",
          "description": "Complement 1q dysfunction (disorder)"
        },
        {
          "id": 535001,
          "code": "234597009",
          "description": "Complement 1r deficiency (disorder)"
        },
        {
          "id": 535002,
          "code": "234598004",
          "description": "Complement 1s deficiency (disorder)"
        },
        {
          "id": 535003,
          "code": "234599007",
          "description": "Complement 2 deficiency (disorder)"
        },
        {
          "id": 535004,
          "code": "234600005",
          "description": "Complement 4 deficiency (disorder)"
        },
        {
          "id": 535005,
          "code": "234601009",
          "description": "Complement 4A deficiency (disorder)"
        },
        {
          "id": 535006,
          "code": "234602002",
          "description": "Complement 4B deficiency (disorder)"
        },
        {
          "id": 535007,
          "code": "234604001",
          "description": "Alternative pathway deficiency (disorder)"
        },
        {
          "id": 535008,
          "code": "234607008",
          "description": "Factor D deficiency (disorder)"
        },
        {
          "id": 535009,
          "code": "234608003",
          "description": "Terminal component deficiency (disorder)"
        },
        {
          "id": 535010,
          "code": "234609006",
          "description": "Complement 5 deficiency (disorder)"
        },
        {
          "id": 535011,
          "code": "234611002",
          "description": "Complement 6 deficiency (disorder)"
        },
        {
          "id": 535012,
          "code": "234612009",
          "description": "Complement 7 deficiency (disorder)"
        },
        {
          "id": 535013,
          "code": "234613004",
          "description": "Combined complement 6 and 7 deficiencies (disorder)"
        },
        {
          "id": 535014,
          "code": "234614005",
          "description": "Complement 8 beta chain deficiency (disorder)"
        },
        {
          "id": 535015,
          "code": "234615006",
          "description": "Complement 8 beta chain dysfunction (disorder)"
        },
        {
          "id": 535016,
          "code": "234616007",
          "description": "Complement 8 alpha-gamma deficiency (disorder)"
        },
        {
          "id": 535017,
          "code": "234617003",
          "description": "Complement 9 deficiency (disorder)"
        },
        {
          "id": 535018,
          "code": "234618008",
          "description": "Complement regulatory factor defect (disorder)"
        },
        {
          "id": 535019,
          "code": "234619000",
          "description": "Hereditary C1 esterase inhibitor deficiency - deficient factor (disorder)"
        },
        {
          "id": 535020,
          "code": "234620006",
          "description": "Hereditary C1 esterase inhibitor deficiency - dysfunctional factor (disorder)"
        },
        {
          "id": 535021,
          "code": "234622003",
          "description": "Factor H deficiency (disorder)"
        },
        {
          "id": 535022,
          "code": "234623008",
          "description": "Complement 4 binding protein deficiency (disorder)"
        },
        {
          "id": 535023,
          "code": "234624002",
          "description": "Decay accelerating factor deficiency (disorder)"
        },
        {
          "id": 535024,
          "code": "234625001",
          "description": "Homologous restriction factor deficiency (disorder)"
        },
        {
          "id": 535025,
          "code": "234626000",
          "description": "Complement 5a inhibitor deficiency (disorder)"
        },
        {
          "id": 535026,
          "code": "234627009",
          "description": "Anaphylotoxin inactivator deficiency (disorder)"
        },
        {
          "id": 535027,
          "code": "234628004",
          "description": "Complement receptor deficiency (disorder)"
        },
        {
          "id": 535028,
          "code": "234629007",
          "description": "Complement receptor 1 deficiency (disorder)"
        },
        {
          "id": 535029,
          "code": "234630002",
          "description": "Complement receptor 3 deficiency (disorder)"
        },
        {
          "id": 535030,
          "code": "234631003",
          "description": "Immunodeficiency with major anomalies (disorder)"
        },
        {
          "id": 535031,
          "code": "234632005",
          "description": "Immunodeficiency associated with chromosomal abnormality (disorder)"
        },
        {
          "id": 535032,
          "code": "234634006",
          "description": "Chromosome 18 syndromes and antibody deficiency (disorder)"
        },
        {
          "id": 535033,
          "code": "234636008",
          "description": "Monosomy 22 and absence of immunoglobulin A (disorder)"
        },
        {
          "id": 535034,
          "code": "234637004",
          "description": "Deletion of X-chromosome and hypogammaglobulinemia (disorder)"
        },
        {
          "id": 535035,
          "code": "234639001",
          "description": "Triple X syndrome, epilepsy, and hypogammaglobulinemia (disorder)"
        },
        {
          "id": 535036,
          "code": "234640004",
          "description": "18-p syndrome with associated immunodeficiency (disorder)"
        },
        {
          "id": 535037,
          "code": "234641000",
          "description": "Immunodeficiency associated with multiple organ system abnormalities (disorder)"
        },
        {
          "id": 535038,
          "code": "234642007",
          "description": "Age-related immunodeficiency (disorder)"
        },
        {
          "id": 535039,
          "code": "234643002",
          "description": "Transient immunodeficiency of infancy (disorder)"
        },
        {
          "id": 535040,
          "code": "234645009",
          "description": "Drug-induced immunodeficiency (disorder)"
        },
        {
          "id": 535041,
          "code": "237989003",
          "description": "Succinate-coenzyme Q reductase deficiency (disorder)"
        },
        {
          "id": 535042,
          "code": "238009001",
          "description": "Adenine phosphoribosyl transferase deficiency type I (disorder)"
        },
        {
          "id": 535043,
          "code": "238010006",
          "description": "Adenine phosphoribosyl transferase deficiency type II (disorder)"
        },
        {
          "id": 535044,
          "code": "24181002",
          "description": "Aplasia of thymus gland with immunodeficiency (disorder)"
        },
        {
          "id": 535045,
          "code": "241955009",
          "description": "Acquired C1 esterase inhibitor deficiency (disorder)"
        },
        {
          "id": 535046,
          "code": "24419001",
          "description": "Disorder of complement (disorder)"
        },
        {
          "id": 535047,
          "code": "24743004",
          "description": "Complement deficiency disease (disorder)"
        },
        {
          "id": 535048,
          "code": "25502009",
          "description": "Episodic lymphocytopenia (disorder)"
        },
        {
          "id": 535049,
          "code": "26252007",
          "description": "Chronic granulomatous disease, type IIA (disorder)"
        },
        {
          "id": 535050,
          "code": "263661007",
          "description": "Complement 5 dysfunction (disorder)"
        },
        {
          "id": 535051,
          "code": "267459007",
          "description": "Deficiencies of humoral immunity (finding)"
        },
        {
          "id": 535052,
          "code": "267460002",
          "description": "Congenital hypogammaglobulinemia (finding)"
        },
        {
          "id": 535053,
          "code": "267543009",
          "description": "Functional disorders of polymorphonuclear neutrophils (disorder)"
        },
        {
          "id": 535054,
          "code": "289317009",
          "description": "Granulocyte granule deficiency (disorder)"
        },
        {
          "id": 535055,
          "code": "29260007",
          "description": "Immunoglobulin A deficiency (disorder)"
        },
        {
          "id": 535056,
          "code": "29272001",
          "description": "Chronic granulomatous disease, type I (disorder)"
        },
        {
          "id": 535057,
          "code": "302874002",
          "description": "Phagocytic cell dysfunction (disorder)"
        },
        {
          "id": 535058,
          "code": "304576008",
          "description": "Metaphyseal chondrodysplasia, McKusick type with associated immunodeficiency (disorder)"
        },
        {
          "id": 535059,
          "code": "31323000",
          "description": "Severe combined immunodeficiency disease (disorder)"
        },
        {
          "id": 535060,
          "code": "319171004",
          "description": "Qualitative abnormality of granulocyte (disorder)"
        },
        {
          "id": 535061,
          "code": "3239007",
          "description": "Lymphocyte disorder (disorder)"
        },
        {
          "id": 535062,
          "code": "33286000",
          "description": "Secondary immune deficiency disorder (disorder)"
        },
        {
          "id": 535063,
          "code": "3439009",
          "description": "Severe combined immunodeficiency due to absent peripheral T cell maturation (disorder)"
        },
        {
          "id": 535064,
          "code": "34916006",
          "description": "Neutrophil motility disorder (disorder)"
        },
        {
          "id": 535065,
          "code": "350353007",
          "description": "De Vaal's syndrome (disorder)"
        },
        {
          "id": 535066,
          "code": "351287008",
          "description": "Reticular dysgenesis with congenital aleukocytosis (disorder)"
        },
        {
          "id": 535067,
          "code": "36070007",
          "description": "Wiskott-Aldrich syndrome (disorder)"
        },
        {
          "id": 535068,
          "code": "36138009",
          "description": "Congenital immunodeficiency disease (disorder)"
        },
        {
          "id": 535069,
          "code": "362993009",
          "description": "Autosomal recessive severe combined immunodeficiency disease (disorder)"
        },
        {
          "id": 535070,
          "code": "363009005",
          "description": "Complement component deficiency (disorder)"
        },
        {
          "id": 535071,
          "code": "363040003",
          "description": "Congenital immunodeficiency involving the hematopoietic system (disorder)"
        },
        {
          "id": 535072,
          "code": "363265005",
          "description": "Predominant humoral immune deficiency (disorder)"
        },
        {
          "id": 535073,
          "code": "36980009",
          "description": "Severe combined immunodeficiency due to absent adenosine deaminase (disorder)"
        },
        {
          "id": 535074,
          "code": "387759001",
          "description": "Chronic granulomatous disease (disorder)"
        },
        {
          "id": 535075,
          "code": "39674000",
          "description": "Familial C3B inhibitor deficiency syndrome (disorder)"
        },
        {
          "id": 535076,
          "code": "40145002",
          "description": "Congenital neutrophil actin dysfunction (disorder)"
        },
        {
          "id": 535077,
          "code": "40197009",
          "description": "Chronic granulomatous disease, type IA (disorder)"
        },
        {
          "id": 535078,
          "code": "402124001",
          "description": "Warts in immune-deficient state (disorder)"
        },
        {
          "id": 535079,
          "code": "402483002",
          "description": "Immunodeficiency with multicarboxylase deficiency (disorder)"
        },
        {
          "id": 535080,
          "code": "402686000",
          "description": "Panniculitis due to immunological disorder (disorder)"
        },
        {
          "id": 535081,
          "code": "402791005",
          "description": "B-lymphocyte immunodeficiency (disorder)"
        },
        {
          "id": 535082,
          "code": "402792003",
          "description": "T-lymphocyte immunodeficiency (disorder)"
        },
        {
          "id": 535083,
          "code": "402794002",
          "description": "Heritable disorder of neutrophil function (disorder)"
        },
        {
          "id": 535084,
          "code": "402900005",
          "description": "Oral hairy leukoplakia associated with immunodeficiency (disorder)"
        },
        {
          "id": 535085,
          "code": "403835002",
          "description": "X-linked hyper-immunoglobulin M syndrome (disorder)"
        },
        {
          "id": 535086,
          "code": "403836001",
          "description": "Autosomal recessive hyperimmunoglobulin M syndrome (disorder)"
        },
        {
          "id": 535087,
          "code": "403837005",
          "description": "Wiskott-Aldrich autosomal dominant variant syndrome (disorder)"
        },
        {
          "id": 535088,
          "code": "403839008",
          "description": "Siccardi syndrome (disorder)"
        },
        {
          "id": 535089,
          "code": "406565005",
          "description": "CD4 T lymphocyte deficiency (disorder)"
        },
        {
          "id": 535090,
          "code": "414395005",
          "description": "Hereditary white blood cell disorder (disorder)"
        },
        {
          "id": 535091,
          "code": "417167007",
          "description": "Immunoglobulin deficiency (disorder)"
        },
        {
          "id": 535092,
          "code": "427167008",
          "description": "Hereditary angioedema with normal C1 esterase inhibitor activity (disorder)"
        },
        {
          "id": 535093,
          "code": "442459007",
          "description": "Combined immunodeficiency disease (disorder)"
        },
        {
          "id": 535094,
          "code": "44306006",
          "description": "T lymphocyte disorder (disorder)"
        },
        {
          "id": 535095,
          "code": "449187006",
          "description": "Kappa light chain deficiency (disorder)"
        },
        {
          "id": 535096,
          "code": "449384005",
          "description": "Lambda light chain deficiency (disorder)"
        },
        {
          "id": 535097,
          "code": "44940001",
          "description": "Adenosine deaminase deficiency (disorder)"
        },
        {
          "id": 535098,
          "code": "449853003",
          "description": "Interleukin-12 deficiency (disorder)"
        },
        {
          "id": 535099,
          "code": "45390000",
          "description": "Severe combined immunodeficiency due to absent interleukin-2 production (disorder)"
        },
        {
          "id": 535100,
          "code": "45841007",
          "description": "Kappa light chain disease (disorder)"
        },
        {
          "id": 535101,
          "code": "47986005",
          "description": "Genetic anomaly of leukocyte (disorder)"
        },
        {
          "id": 535102,
          "code": "48119005",
          "description": "Dysplasia of thymus gland with immunodeficiency (disorder)"
        },
        {
          "id": 535103,
          "code": "49555001",
          "description": "Severe combined immunodeficiency due to absent T cell receptor (disorder)"
        },
        {
          "id": 535104,
          "code": "50926003",
          "description": "Job's syndrome (disorder)"
        },
        {
          "id": 535105,
          "code": "51319002",
          "description": "Light chain disease (disorder)"
        },
        {
          "id": 535106,
          "code": "55602000",
          "description": "Nezelof's syndrome (disorder)"
        },
        {
          "id": 535107,
          "code": "58606001",
          "description": "Primary immune deficiency disorder (disorder)"
        },
        {
          "id": 535108,
          "code": "60743005",
          "description": "Purine-nucleoside phosphorylase deficiency (disorder)"
        },
        {
          "id": 535109,
          "code": "65880007",
          "description": "X-linked agammaglobulinemia (disorder)"
        },
        {
          "id": 535110,
          "code": "66876008",
          "description": "Lambda light chain disease (disorder)"
        },
        {
          "id": 535111,
          "code": "699869003",
          "description": "Interleukin-1 receptor-associated kinase 4 deficiency (disorder)"
        },
        {
          "id": 535112,
          "code": "703525006",
          "description": "Anhidrotic ectodermal dysplasia with immune deficiency (disorder)"
        },
        {
          "id": 535113,
          "code": "703538003",
          "description": "Mannose-binding lectin deficiency (disorder)"
        },
        {
          "id": 535114,
          "code": "707152007",
          "description": "Phagocytic immunodeficiency (disorder)"
        },
        {
          "id": 535115,
          "code": "710735009",
          "description": "Periodontitis co-occurrent with leukocyte adhesion deficiency (disorder)"
        },
        {
          "id": 535116,
          "code": "711160007",
          "description": "Eosinophil peroxidase deficiency (disorder)"
        },
        {
          "id": 535117,
          "code": "711480000",
          "description": "Activated PI3K-delta syndrome (disorder)"
        },
        {
          "id": 535118,
          "code": "711481001",
          "description": "X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia (disorder)"
        },
        {
          "id": 535119,
          "code": "71436005",
          "description": "Lazy leukocyte syndrome (disorder)"
        },
        {
          "id": 535120,
          "code": "715982006",
          "description": "Severe combined immunodeficiency due to deoxyribonucleic acid cross-link repair protein 1c deficiency (disorder)"
        },
        {
          "id": 535121,
          "code": "716378008",
          "description": "Combined immunodeficiency due to Zeta-chain associated protein kinase 70 deficiency (disorder)"
        },
        {
          "id": 535122,
          "code": "716766007",
          "description": "Malakoplakia (disorder)"
        },
        {
          "id": 535123,
          "code": "716869006",
          "description": "Mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency (disorder)"
        },
        {
          "id": 535124,
          "code": "716871006",
          "description": "Severe combined immunodeficiency due to deoxyribonucleic acid dependent protein kinase catalytic subunit deficiency (disorder)"
        },
        {
          "id": 535125,
          "code": "717811007",
          "description": "Combined immunodeficiency due to calcium release activated calcium channel dysfunction (disorder)"
        },
        {
          "id": 535126,
          "code": "718107000",
          "description": "Severe combined immunodeficiency T-cell negative B-cell positive due to janus kinase-3 deficiency (disorder)"
        },
        {
          "id": 535127,
          "code": "718230004",
          "description": "Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency (disorder)"
        },
        {
          "id": 535128,
          "code": "718232007",
          "description": "Pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 (disorder)"
        },
        {
          "id": 535129,
          "code": "718717004",
          "description": "Primary immunodeficiency syndrome due to p14 deficiency (disorder)"
        },
        {
          "id": 535130,
          "code": "71904008",
          "description": "Severe combined immunodeficiency due to absent class II human leukocyte antigens (disorder)"
        },
        {
          "id": 535131,
          "code": "719685004",
          "description": "Absent thumb with short stature and immunodeficiency syndrome (disorder)"
        },
        {
          "id": 535132,
          "code": "719814009",
          "description": "X-linked mendelian susceptibility to mycobacterial disease (disorder)"
        },
        {
          "id": 535133,
          "code": "719827008",
          "description": "X-linked immunoneurologic disorder (disorder)"
        },
        {
          "id": 535134,
          "code": "720345008",
          "description": "Severe T-cell immunodeficiency, congenital alopecia, nail dystrophy syndrome (disorder)"
        },
        {
          "id": 535135,
          "code": "720853005",
          "description": "Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome (disorder)"
        },
        {
          "id": 535136,
          "code": "721876004",
          "description": "Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 2 deficiency (disorder)"
        },
        {
          "id": 535137,
          "code": "721877008",
          "description": "Mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency (disorder)"
        },
        {
          "id": 535138,
          "code": "721977007",
          "description": "Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome (disorder)"
        },
        {
          "id": 535139,
          "code": "722067005",
          "description": "Severe combined immunodeficiency with hypereosinophilia (disorder)"
        },
        {
          "id": 535140,
          "code": "723334006",
          "description": "Immunodeficiency due to mutation of FAS-associated protein with death domain gene (disorder)"
        },
        {
          "id": 535141,
          "code": "723384004",
          "description": "Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency (disorder)"
        },
        {
          "id": 535142,
          "code": "723385003",
          "description": "Mendelian susceptibility to mycobacterial disease due to partial interferon regulatory factor 8 deficiency (disorder)"
        },
        {
          "id": 535143,
          "code": "723386002",
          "description": "Mendelian susceptibility to mycobacterial disease due to partial signal transducer and activator of transcription 1 deficiency (disorder)"
        },
        {
          "id": 535144,
          "code": "723443003",
          "description": "Neutrophil immunodeficiency syndrome (disorder)"
        },
        {
          "id": 535145,
          "code": "724177005",
          "description": "Ligase 4 syndrome (disorder)"
        },
        {
          "id": 535146,
          "code": "724179008",
          "description": "Laron syndrome with immunodeficiency (disorder)"
        },
        {
          "id": 535147,
          "code": "724275005",
          "description": "Primary immunodeficiency with natural killer cell deficiency and adrenal insufficiency (disorder)"
        },
        {
          "id": 535148,
          "code": "724361001",
          "description": "Hepatic veno-occlusive disease with immunodeficiency syndrome (disorder)"
        },
        {
          "id": 535149,
          "code": "725135004",
          "description": "Combined immunodeficiency due to CD3gamma deficiency (disorder)"
        },
        {
          "id": 535150,
          "code": "725136003",
          "description": "Immunodeficiency by defective expression of human leukocyte antigen class 1 (disorder)"
        },
        {
          "id": 535151,
          "code": "725137007",
          "description": "Neutropenia, monocytopenia, deafness syndrome (disorder)"
        },
        {
          "id": 535152,
          "code": "725150008",
          "description": "Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency (disorder)"
        },
        {
          "id": 535153,
          "code": "725151007",
          "description": "Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency (disorder)"
        },
        {
          "id": 535154,
          "code": "725290000",
          "description": "Combined immunodeficiency due to partial recombination-activating gene 1 deficiency (disorder)"
        },
        {
          "id": 535155,
          "code": "725431001",
          "description": "Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency (disorder)"
        },
        {
          "id": 535156,
          "code": "725432008",
          "description": "Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency (disorder)"
        },
        {
          "id": 535157,
          "code": "735436001",
          "description": "Acquired disorder of neutrophil function (disorder)"
        },
        {
          "id": 535158,
          "code": "735437005",
          "description": "Disorder of neutrophil adhesion (disorder)"
        },
        {
          "id": 535159,
          "code": "735438000",
          "description": "Disorder of neutrophil chemotaxis (disorder)"
        },
        {
          "id": 535160,
          "code": "735536003",
          "description": "Adult-onset immunodeficiency (disorder)"
        },
        {
          "id": 535161,
          "code": "737307003",
          "description": "Natural-killer cell deficiency (disorder)"
        },
        {
          "id": 535162,
          "code": "76243000",
          "description": "Chronic granulomatous disease, type IVA (disorder)"
        },
        {
          "id": 535163,
          "code": "763623001",
          "description": "Severe combined immunodeficiency due to cytidine 5-prime triphosphate synthetase 1 deficiency (disorder)"
        },
        {
          "id": 535164,
          "code": "763668009",
          "description": "Lichtenstein syndrome (disorder)"
        },
        {
          "id": 535165,
          "code": "763713000",
          "description": "Idiopathic CD4 lymphocytopenia (disorder)"
        },
        {
          "id": 535166,
          "code": "764858009",
          "description": "Isolated agammaglobulinemia (disorder)"
        },
        {
          "id": 535167,
          "code": "764946008",
          "description": "Constitutional mismatch repair deficiency syndrome (disorder)"
        },
        {
          "id": 535168,
          "code": "765145001",
          "description": "T cell negative B cell positive severe combined immunodeficiency due to gamma chain deficiency (disorder)"
        },
        {
          "id": 535169,
          "code": "765188009",
          "description": "Severe combined immunodeficiency due to complete recombination-activating gene 1 and/or recombination-activating gene 2 deficiency (disorder)"
        },
        {
          "id": 535170,
          "code": "766705006",
          "description": "Immunodeficiency due to ficolin 3 deficiency (disorder)"
        },
        {
          "id": 535171,
          "code": "766879006",
          "description": "Combined immunodeficiency due to OX40 deficiency (disorder)"
        },
        {
          "id": 535172,
          "code": "766983005",
          "description": "Susceptibility to respiratory infection associated with CD8alpha chain mutation (disorder)"
        },
        {
          "id": 535173,
          "code": "767263007",
          "description": "22q11.2 deletion syndrome (disorder)"
        },
        {
          "id": 535174,
          "code": "768560008",
          "description": "Melanoma differentiation-associated gene 5 deficiency (disorder)"
        },
        {
          "id": 535175,
          "code": "770785002",
          "description": "T-cell immunodeficiency due to ras homolog family member H deficiency (disorder)"
        },
        {
          "id": 535176,
          "code": "771078002",
          "description": "Immunodeficiency due to mannan binding lectin serine peptidase 2 deficiency (disorder)"
        },
        {
          "id": 535177,
          "code": "77121009",
          "description": "X-linked lymphoproliferative syndrome (disorder)"
        },
        {
          "id": 535178,
          "code": "771443008",
          "description": "Complement component 3 deficiency (disorder)"
        },
        {
          "id": 535179,
          "code": "771479000",
          "description": "Combined immunodeficiency due to serine/threonine kinase 4 deficiency (disorder)"
        },
        {
          "id": 535180,
          "code": "771517009",
          "description": "Severe combined immunodeficiency due to caspase recruitment domain family member 11 deficiency (disorder)"
        },
        {
          "id": 535181,
          "code": "772126000",
          "description": "Poikiloderma with neutropenia (disorder)"
        },
        {
          "id": 535182,
          "code": "77330006",
          "description": "Chronic granulomatous disease, type II (disorder)"
        },
        {
          "id": 535183,
          "code": "773488000",
          "description": "Combined immunodeficiency due to mucosa-associated lymphoid tissue lymphoma translocation gene 1 deficiency (disorder)"
        },
        {
          "id": 535184,
          "code": "773730002",
          "description": "Osteopetrosis hypogammaglobulinemia syndrome (disorder)"
        },
        {
          "id": 535185,
          "code": "778004006",
          "description": "Autoinflammation phospholipase C gamma 2 associated antibody deficiency and immune dysregulation (disorder)"
        },
        {
          "id": 535186,
          "code": "778024005",
          "description": "Monocytopenia with susceptibility to infections (disorder)"
        },
        {
          "id": 535187,
          "code": "778027003",
          "description": "Primary CD59 deficiency (disorder)"
        },
        {
          "id": 535188,
          "code": "778028008",
          "description": "Immunodeficiency due to CD25 deficiency (disorder)"
        },
        {
          "id": 535189,
          "code": "778045003",
          "description": "Susceptibility to viral and mycobacterial infection (disorder)"
        },
        {
          "id": 535190,
          "code": "782750002",
          "description": "T-cell receptor alpha-beta-positive T-cell deficiency (disorder)"
        },
        {
          "id": 535191,
          "code": "782751003",
          "description": "Severe combined immunodeficiency due to inhibitor of nuclear factor kappa B kinase subunit beta deficiency (disorder)"
        },
        {
          "id": 535192,
          "code": "783007005",
          "description": "Recurrent Neisseria infection due to factor D deficiency (disorder)"
        },
        {
          "id": 535193,
          "code": "783099001",
          "description": "Radiosensitivity, immunodeficiency, dysmorphic features, learning difficulties syndrome (disorder)"
        },
        {
          "id": 535194,
          "code": "783142006",
          "description": "Pancytopenia due to IKAROS family zinc finger 1 mutations (disorder)"
        },
        {
          "id": 535195,
          "code": "783205005",
          "description": "Alopecia antibody deficiency (disorder)"
        },
        {
          "id": 535196,
          "code": "783245001",
          "description": "Primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection (disorder)"
        },
        {
          "id": 535197,
          "code": "783248004",
          "description": "Hyperimmunoglobulin M syndrome with susceptibility to opportunistic infection (disorder)"
        },
        {
          "id": 535198,
          "code": "783249007",
          "description": "Hyperimmunoglobulin M syndrome without susceptibility to opportunistic infection (disorder)"
        },
        {
          "id": 535199,
          "code": "783617001",
          "description": "Severe combined immunodeficiency due to lymphocyte-specific protein-tyrosine kinase deficiency (disorder)"
        },
        {
          "id": 535200,
          "code": "783621008",
          "description": "Immunodeficiency with factor I anomaly (disorder)"
        },
        {
          "id": 535201,
          "code": "783743009",
          "description": "Combined immunodeficiency with granulomatosis (disorder)"
        },
        {
          "id": 535202,
          "code": "784340000",
          "description": "Combined immunodeficiency due to interleukin 21 receptor deficiency (disorder)"
        },
        {
          "id": 535203,
          "code": "784393004",
          "description": "Adult-onset immunodeficiency with anti-interferon-gamma autoantibodies (disorder)"
        },
        {
          "id": 535204,
          "code": "789777007",
          "description": "Short-limb skeletal dysplasia with severe combined immunodeficiency (disorder)"
        },
        {
          "id": 535205,
          "code": "81166004",
          "description": "Properdin deficiency disease (disorder)"
        },
        {
          "id": 535206,
          "code": "82286005",
          "description": "Hyperimmunoglobulin M syndrome (disorder)"
        },
        {
          "id": 535207,
          "code": "82317007",
          "description": "Chronic granulomatous disease, type III (disorder)"
        },
        {
          "id": 535208,
          "code": "82966003",
          "description": "Hereditary angioedema (disorder)"
        },
        {
          "id": 535209,
          "code": "840435003",
          "description": "Disseminated dermatophytosis due to immunodeficiency (disorder)"
        },
        {
          "id": 535210,
          "code": "840472009",
          "description": "Deficiency of immunoglobulin A with immunoglobulin G subclass deficiency (disorder)"
        },
        {
          "id": 535211,
          "code": "9893005",
          "description": "Immunodeficiency with thymoma (disorder)"
        }
      ]
    }
  ],
  "version_history": [
    {
      "version_id": 11514,
      "version_name": "Immunological (SNOMED-CT)",
      "version_date": "2025-01-19T16:22:03.984974Z",
      "is_published": true,
      "is_latest": true
    }
  ]
}