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FHIR IG Statistics: ValueSet/2.16.840.1.114222.4.11.3060

Packageus.cdc.phinvads
Resource TypeValueSet
Id2.16.840.1.114222.4.11.3060
FHIR VersionR4
Sourcehttp://fhir.org/packages/us.cdc.phinvads
URLhttp://phinvads.cdc.gov/fhir/ValueSet/2.16.840.1.114222.4.11.3060
Version6
Statusactive
Date2019-01-15T00:04:00+11:00
NamePHVS_ImmunosuppressedCondition_CDC
TitleImmunosuppressed Condition
Realmus
DescriptionImmunosuppressed conditions answer list based on SNOMED domain (234532001)

Resources that use this resource

No resources found


Resources that this resource uses

CodeSystem
sctSNOMED CT (all versions)

Narrative

No narrative content found in resource


Source

{
  "resourceType": "ValueSet",
  "id": "2.16.840.1.114222.4.11.3060",
  "meta": {
    "source": "https://phinvads.cdc.gov/vads/ViewValueSet.action?oid=2.16.840.1.114222.4.11.3060"
  },
  "url": "http://phinvads.cdc.gov/fhir/ValueSet/2.16.840.1.114222.4.11.3060",
  "version": "6",
  "name": "PHVS_ImmunosuppressedCondition_CDC",
  "title": "Immunosuppressed Condition",
  "status": "active",
  "date": "2019-01-15T00:04:00+11:00",
  "description": "Immunosuppressed conditions answer list based on SNOMED domain (234532001)",
  "compose": {
    "include": [
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20200901",
        "concept": [
          {
            "code": "234640004",
            "display": "18-p syndrome with associated immunodeficiency (disorder)"
          },
          {
            "code": "719685004",
            "display": "Absent thumb with short stature and immunodeficiency syndrome (disorder)"
          },
          {
            "code": "62479008",
            "display": "Acquired immune deficiency syndrome (disorder)"
          },
          {
            "code": "10746341000119109",
            "display": "Acquired immune deficiency syndrome complicating childbirth (disorder)"
          },
          {
            "code": "735434003",
            "display": "Acquired neutrophilia (disorder)"
          },
          {
            "code": "711480000",
            "display": "Activated PI3K-delta syndrome (disorder)"
          },
          {
            "code": "47144000",
            "display": "Acute neutrophilia (disorder)"
          },
          {
            "code": "44940001",
            "display": "Adenosine deaminase deficiency (disorder)"
          },
          {
            "code": "735536003",
            "display": "Adult-onset immunodeficiency (disorder)"
          },
          {
            "code": "722281001",
            "display": "Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome (disorder)"
          },
          {
            "code": "234642007",
            "display": "Age-related immunodeficiency (disorder)"
          },
          {
            "code": "17182001",
            "display": "Agranulocytosis (disorder)"
          },
          {
            "code": "421312009",
            "display": "Agranulocytosis associated with acquired immunodeficiency syndrome (disorder)"
          },
          {
            "code": "713530002",
            "display": "Agranulocytosis co-occurrent with human immunodeficiency virus infection (disorder)"
          },
          {
            "code": "14333004",
            "display": "Alloimmune neonatal neutropenia (disorder)"
          },
          {
            "code": "234604001",
            "display": "Alternative pathway deficiency (disorder)"
          },
          {
            "code": "234627009",
            "display": "Anaphylotoxin inactivator deficiency (disorder)"
          },
          {
            "code": "703525006",
            "display": "Anhidrotic ectodermal dysplasia with immune deficiency (disorder)"
          },
          {
            "code": "720986005",
            "display": "Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome (disorder)"
          },
          {
            "code": "234558001",
            "display": "Anti-haemophilus influenzae B polysaccharide antibody deficiency (disorder)"
          },
          {
            "code": "234560004",
            "display": "Anti-meningococcal polysaccharide A antibody deficiency (disorder)"
          },
          {
            "code": "234561000",
            "display": "Anti-meningococcal polysaccharide C antibody deficiency (disorder)"
          },
          {
            "code": "234559009",
            "display": "Anti-pneumococcal polysaccharide antibody deficiency (disorder)"
          },
          {
            "code": "234557006",
            "display": "Anti-polysaccharide antibody deficiency (disorder)"
          },
          {
            "code": "234562007",
            "display": "Anti-protein antibody deficiency (disorder)"
          },
          {
            "code": "234563002",
            "display": "Anti-staphylococcal antibody deficiency (disorder)"
          },
          {
            "code": "24181002",
            "display": "Aplasia of thymus gland with immunodeficiency (disorder)"
          },
          {
            "code": "68504005",
            "display": "Ataxia-telangiectasia syndrome (disorder)"
          },
          {
            "code": "720520009",
            "display": "Attenuated Ch+¬diak-Higashi syndrome (disorder)"
          },
          {
            "code": "722288007",
            "display": "Autoimmune enteropathy and endocrinopathy with susceptibility to chronic infection syndrome (disorder)"
          },
          {
            "code": "722290008",
            "display": "Autoimmune lymphoproliferative syndrome with recurrent viral infection (disorder)"
          },
          {
            "code": "234425008",
            "display": "Autoimmune neutropenia (disorder)"
          },
          {
            "code": "234534000",
            "display": "Autosomal agammaglobulinemia with absent B-cells (disorder)"
          },
          {
            "code": "725150008",
            "display": "Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency (disorder)"
          },
          {
            "code": "725151007",
            "display": "Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency (disorder)"
          },
          {
            "code": "770947009",
            "display": "Autosomal dominant severe congenital neutropenia (disorder)"
          },
          {
            "code": "403836001",
            "display": "Autosomal recessive hyperimmunoglobulin M syndrome (disorder)"
          },
          {
            "code": "771309000",
            "display": "Autosomal recessive lymphoproliferative disease (disorder)"
          },
          {
            "code": "725431001",
            "display": "Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency (disorder)"
          },
          {
            "code": "725432008",
            "display": "Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency (disorder)"
          },
          {
            "code": "190993005",
            "display": "Autosomal recessive severe combined immunodeficiency (disorder)"
          },
          {
            "code": "362993009",
            "display": "Autosomal recessive severe combined immunodeficiency disease (disorder)"
          },
          {
            "code": "234572005",
            "display": "Benign combined immunodeficiency (disorder)"
          },
          {
            "code": "129640007",
            "display": "Benign granulocytopenia in childhood (disorder)"
          },
          {
            "code": "4434006",
            "display": "Bloom syndrome (disorder)"
          },
          {
            "code": "402791005",
            "display": "B-lymphocyte immunodeficiency (disorder)"
          },
          {
            "code": "234633000",
            "display": "Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency (disorder)"
          },
          {
            "code": "111396008",
            "display": "Ch+¬diak-Higashi syndrome (disorder)"
          },
          {
            "code": "276628009",
            "display": "Chloramphenicol-induced neutropenia (disorder)"
          },
          {
            "code": "234634006",
            "display": "Chromosome 18 syndromes and antibody deficiency (disorder)"
          },
          {
            "code": "234635007",
            "display": "Chromosome 22 abnormalities with hypogammaglobulinemia (disorder)"
          },
          {
            "code": "234418001",
            "display": "Chronic benign granulocytopenia (disorder)"
          },
          {
            "code": "234423001",
            "display": "Chronic benign neutropenia (disorder)"
          },
          {
            "code": "129641006",
            "display": "Chronic benign neutropenia of childhood (disorder)"
          },
          {
            "code": "234576008",
            "display": "Chronic familial neutropaenia (disorder)"
          },
          {
            "code": "387759001",
            "display": "Chronic granulomatous disease (disorder)"
          },
          {
            "code": "29272001",
            "display": "Chronic granulomatous disease, type I (disorder)"
          },
          {
            "code": "40197009",
            "display": "Chronic granulomatous disease, type IA (disorder)"
          },
          {
            "code": "77330006",
            "display": "Chronic granulomatous disease, type II (disorder)"
          },
          {
            "code": "26252007",
            "display": "Chronic granulomatous disease, type IIA (disorder)"
          },
          {
            "code": "82317007",
            "display": "Chronic granulomatous disease, type III (disorder)"
          },
          {
            "code": "21527007",
            "display": "Chronic granulomatous disease, type IV (disorder)"
          },
          {
            "code": "76243000",
            "display": "Chronic granulomatous disease, type IVA (disorder)"
          },
          {
            "code": "129643009",
            "display": "Chronic hypoplastic neutropenia (disorder)"
          },
          {
            "code": "129642004",
            "display": "Chronic idiopathic immunoneutropenia in adults (disorder)"
          },
          {
            "code": "248693006",
            "display": "Chronic idiopathic neutropenia (disorder)"
          },
          {
            "code": "80369006",
            "display": "Chronic neutrophilia (disorder)"
          },
          {
            "code": "234593008",
            "display": "Classical complement pathway abnormality (disorder)"
          },
          {
            "code": "234613004",
            "display": "Combined complement 6 and 7 deficiencies (disorder)"
          },
          {
            "code": "442459007",
            "display": "Combined immunodeficiency disease (disorder)"
          },
          {
            "code": "717811007",
            "display": "Combined immunodeficiency due to calcium release activated calcium channel dysfunction (disorder)"
          },
          {
            "code": "725135004",
            "display": "Combined immunodeficiency due to CD3gamma deficiency (disorder)"
          },
          {
            "code": "773488000",
            "display": "Combined immunodeficiency due to mucosa-associated lymphoid tissue lymphoma translocation gene 1 deficiency (disorder)"
          },
          {
            "code": "766879006",
            "display": "Combined immunodeficiency due to OX40 deficiency (disorder)"
          },
          {
            "code": "725290000",
            "display": "Combined immunodeficiency due to partial recombination-activating gene 1 deficiency (disorder)"
          },
          {
            "code": "771479000",
            "display": "Combined immunodeficiency due to serine/threonine kinase 4 deficiency (disorder)"
          },
          {
            "code": "716378008",
            "display": "Combined immunodeficiency due to Zeta-chain associated protein kinase 70 deficiency (disorder)"
          },
          {
            "code": "770625006",
            "display": "Combined immunodeficiency with faciooculoskeletal anomalies syndrome (disorder)"
          },
          {
            "code": "234547005",
            "display": "Combined immunoglobulin G2 and G4 deficiency (disorder)"
          },
          {
            "code": "234591005",
            "display": "Combined phagocytic defect (disorder)"
          },
          {
            "code": "23238000",
            "display": "Common variable agammaglobulinemia (disorder)"
          },
          {
            "code": "191013002",
            "display": "Common variable immunodeficiency with autoantibodies to B- or T-cells (disorder)"
          },
          {
            "code": "191011000",
            "display": "Common variable immunodeficiency with predominant abnormalities of B-cell numbers and functions (disorder)"
          },
          {
            "code": "191012007",
            "display": "Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder)"
          },
          {
            "code": "234595001",
            "display": "Complement 1q beta chain deficiency (disorder)"
          },
          {
            "code": "234594002",
            "display": "Complement 1q deficiency (disorder)"
          },
          {
            "code": "234596000",
            "display": "Complement 1q dysfunction (disorder)"
          },
          {
            "code": "234597009",
            "display": "Complement 1r deficiency (disorder)"
          },
          {
            "code": "234598004",
            "display": "Complement 1s deficiency (disorder)"
          },
          {
            "code": "234599007",
            "display": "Complement 2 deficiency (disorder)"
          },
          {
            "code": "234603007",
            "display": "Complement 3 deficiency (disorder)"
          },
          {
            "code": "234623008",
            "display": "Complement 4 binding protein deficiency (disorder)"
          },
          {
            "code": "234600005",
            "display": "Complement 4 deficiency (disorder)"
          },
          {
            "code": "234601009",
            "display": "Complement 4A deficiency (disorder)"
          },
          {
            "code": "234602002",
            "display": "Complement 4B deficiency (disorder)"
          },
          {
            "code": "234609006",
            "display": "Complement 5 deficiency (disorder)"
          },
          {
            "code": "263661007",
            "display": "Complement 5 dysfunction (disorder)"
          },
          {
            "code": "234626000",
            "display": "Complement 5a inhibitor deficiency (disorder)"
          },
          {
            "code": "234611002",
            "display": "Complement 6 deficiency (disorder)"
          },
          {
            "code": "234612009",
            "display": "Complement 7 deficiency (disorder)"
          },
          {
            "code": "234616007",
            "display": "Complement 8 alpha-gamma deficiency (disorder)"
          },
          {
            "code": "234614005",
            "display": "Complement 8 beta chain deficiency (disorder)"
          },
          {
            "code": "234615006",
            "display": "Complement 8 beta chain dysfunction (disorder)"
          },
          {
            "code": "234617003",
            "display": "Complement 9 deficiency (disorder)"
          },
          {
            "code": "18827005",
            "display": "Complement abnormality (disorder)"
          },
          {
            "code": "771443008",
            "display": "Complement component 3 deficiency (disorder)"
          },
          {
            "code": "363009005",
            "display": "Complement component deficiency (disorder)"
          },
          {
            "code": "24743004",
            "display": "Complement deficiency disease (disorder)"
          },
          {
            "code": "234629007",
            "display": "Complement receptor 1 deficiency (disorder)"
          },
          {
            "code": "234630002",
            "display": "Complement receptor 3 deficiency (disorder)"
          },
          {
            "code": "234628004",
            "display": "Complement receptor deficiency (disorder)"
          },
          {
            "code": "234618008",
            "display": "Complement regulatory factor defect (disorder)"
          },
          {
            "code": "116133005",
            "display": "Congenital agammaglobulinemia (disorder)"
          },
          {
            "code": "58034007",
            "display": "Congenital hypergammaglobulinemia (disorder)"
          },
          {
            "code": "36138009",
            "display": "Congenital immunodeficiency disease (disorder)"
          },
          {
            "code": "363040003",
            "display": "Congenital immunodeficiency involving the hematopoietic system (disorder)"
          },
          {
            "code": "77358003",
            "display": "Congenital leukocyte adherence deficiency (disorder)"
          },
          {
            "code": "89655007",
            "display": "Congenital neutropenia (disorder)"
          },
          {
            "code": "775909002",
            "display": "Congenital neutropenia, myelofibrosis, nephromegaly syndrome (disorder)"
          },
          {
            "code": "765327005",
            "display": "Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome (disorder)"
          },
          {
            "code": "764946008",
            "display": "Constitutional mismatch repair deficiency syndrome (disorder)"
          },
          {
            "code": "735435002",
            "display": "Constitutional neutrophilia (disorder)"
          },
          {
            "code": "234426009",
            "display": "Corticosteroid-induced neutrophilia (disorder)"
          },
          {
            "code": "191347008",
            "display": "Cyclical neutropenia (disorder)"
          },
          {
            "code": "350353007",
            "display": "De Vaal's syndrome (disorder)"
          },
          {
            "code": "234624002",
            "display": "Decay accelerating factor deficiency (disorder)"
          },
          {
            "code": "234555003",
            "display": "Defective immunoglobulin glycosylation (disorder)"
          },
          {
            "code": "234581004",
            "display": "Defective phagocytic cell adhesion (disorder)"
          },
          {
            "code": "234580003",
            "display": "Defective phagocytic cell chemotaxis (disorder)"
          },
          {
            "code": "234585008",
            "display": "Defective phagocytic cell killing (disorder)"
          },
          {
            "code": "234578009",
            "display": "Defective phagocytic cell opsonization (disorder)"
          },
          {
            "code": "773664005",
            "display": "Deficiency in anterior pituitary function, variable immunodeficiency syndrome (disorder)"
          },
          {
            "code": "234637004",
            "display": "Deletion of X-chromosome and hypogammaglobulinemia (disorder)"
          },
          {
            "code": "24419001",
            "display": "Disorder of complement (disorder)"
          },
          {
            "code": "234574006",
            "display": "Disorder of phagocytic cell number (disorder)"
          },
          {
            "code": "56918001",
            "display": "Dose-related drug-induced neutropenia (disorder)"
          },
          {
            "code": "234645009",
            "display": "Drug-induced immunodeficiency (disorder)"
          },
          {
            "code": "47318007",
            "display": "Drug-induced neutropenia (disorder)"
          },
          {
            "code": "63484008",
            "display": "Drug-induced neutrophilia (disorder)"
          },
          {
            "code": "48119005",
            "display": "Dysplasia of thymus gland with immunodeficiency (disorder)"
          },
          {
            "code": "771515001",
            "display": "Facial dysmorphism, immunodeficiency, livedo, short stature syndrome (disorder)"
          },
          {
            "code": "234605000",
            "display": "Factor B deficiency (disorder)"
          },
          {
            "code": "234607008",
            "display": "Factor D deficiency (disorder)"
          },
          {
            "code": "234622003",
            "display": "Factor H deficiency (disorder)"
          },
          {
            "code": "234621005",
            "display": "Factor I deficiency (disorder)"
          },
          {
            "code": "39674000",
            "display": "Familial C3B inhibitor deficiency syndrome (disorder)"
          },
          {
            "code": "699861000",
            "display": "Familial granulomatous inflammatory arthritis, dermatitis and uveitis (disorder)"
          },
          {
            "code": "398250003",
            "display": "Familial hemophagocytic lymphohistiocytosis (disorder)"
          },
          {
            "code": "234566005",
            "display": "Familial immunoglobulin hypercatabolism (disorder)"
          },
          {
            "code": "247860002",
            "display": "Familial neutropenia (disorder)"
          },
          {
            "code": "426800001",
            "display": "Febrile granulocytopenia (disorder)"
          },
          {
            "code": "409089005",
            "display": "Febrile neutropenia (disorder)"
          },
          {
            "code": "267543009",
            "display": "Functional disorders of polymorphonuclear neutrophils (disorder)"
          },
          {
            "code": "234590006",
            "display": "Gluthathione peroxidase deficiency (disorder)"
          },
          {
            "code": "234589002",
            "display": "Gluthathione synthetase deficiency (disorder)"
          },
          {
            "code": "417672002",
            "display": "Granulocytopenic disorder (disorder)"
          },
          {
            "code": "234436001",
            "display": "Hemolytic erythrophagocytic syndrome (disorder)"
          },
          {
            "code": "234437005",
            "display": "Hemophagocytic lymphohistiocytosis (disorder)"
          },
          {
            "code": "713444005",
            "display": "Hemophagocytic syndrome co-occurrent with human immunodeficiency virus infection (disorder)"
          },
          {
            "code": "190959006",
            "display": "Hemophagocytic syndrome, infection-associated (disorder)"
          },
          {
            "code": "724361001",
            "display": "Hepatic veno-occlusive disease with immunodeficiency syndrome (disorder)"
          },
          {
            "code": "82966003",
            "display": "Hereditary angioedema (disorder)"
          },
          {
            "code": "427167008",
            "display": "Hereditary angioedema with normal C1 esterase inhibitor activity (disorder)"
          },
          {
            "code": "234619000",
            "display": "Hereditary C1 esterase inhibitor deficiency - deficient factor (disorder)"
          },
          {
            "code": "234620006",
            "display": "Hereditary C1 esterase inhibitor deficiency - dysfunctional factor (disorder)"
          },
          {
            "code": "129639005",
            "display": "Hereditary neutrophilia (finding)"
          },
          {
            "code": "234625001",
            "display": "Homologous restriction factor deficiency (disorder)"
          },
          {
            "code": "82286005",
            "display": "Hyperimmunoglobulin M syndrome (disorder)"
          },
          {
            "code": "37548006",
            "display": "Hypopigmentation-immunodeficiency disease (disorder)"
          },
          {
            "code": "763713000",
            "display": "Idiopathic CD4 lymphocytopenia (disorder)"
          },
          {
            "code": "771333006",
            "display": "Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection syndrome (disorder)"
          },
          {
            "code": "65623009",
            "display": "Immune neutropenia (disorder)"
          },
          {
            "code": "234632005",
            "display": "Immunodeficiency associated with chromosomal abnormality (disorder)"
          },
          {
            "code": "234641000",
            "display": "Immunodeficiency associated with multiple organ system abnormalities (disorder)"
          },
          {
            "code": "725136003",
            "display": "Immunodeficiency by defective expression of human leukocyte antigen class 1 (disorder)"
          },
          {
            "code": "103079001",
            "display": "Immunodeficiency caused by corticosteroid (disorder)"
          },
          {
            "code": "10838971000119103",
            "display": "Immunodeficiency caused by long term therapeutic use of drug (disorder)"
          },
          {
            "code": "234532001",
            "display": "Immunodeficiency disorder (disorder)"
          },
          {
            "code": "778028008",
            "display": "Immunodeficiency due to CD25 deficiency (disorder)"
          },
          {
            "code": "766705006",
            "display": "Immunodeficiency due to ficolin 3 deficiency (disorder)"
          },
          {
            "code": "771078002",
            "display": "Immunodeficiency due to mannan binding lectin serine peptidase 2 deficiency (disorder)"
          },
          {
            "code": "723334006",
            "display": "Immunodeficiency due to mutation of FAS-associated protein with death domain gene (disorder)"
          },
          {
            "code": "191008001",
            "display": "Immunodeficiency following hereditary defective response to Epstein-Barr virus (disorder)"
          },
          {
            "code": "103081004",
            "display": "Immunodeficiency secondary to chemotherapy (disorder)"
          },
          {
            "code": "103077004",
            "display": "Immunodeficiency secondary to neoplasm (disorder)"
          },
          {
            "code": "103080003",
            "display": "Immunodeficiency secondary to radiation therapy (disorder)"
          },
          {
            "code": "103078009",
            "display": "Immunodeficiency secondary to trauma (disorder)"
          },
          {
            "code": "234631003",
            "display": "Immunodeficiency with major anomalies (disorder)"
          },
          {
            "code": "402483002",
            "display": "Immunodeficiency with multicarboxylase deficiency (disorder)"
          },
          {
            "code": "9893005",
            "display": "Immunodeficiency with thymoma (disorder)"
          },
          {
            "code": "29260007",
            "display": "Immunoglobulin A deficiency (disorder)"
          },
          {
            "code": "234551007",
            "display": "Immunoglobulin A1 deficiency (disorder)"
          },
          {
            "code": "234552000",
            "display": "Immunoglobulin A2 deficiency (disorder)"
          },
          {
            "code": "417167007",
            "display": "Immunoglobulin deficiency (disorder)"
          },
          {
            "code": "12631000119106",
            "display": "Immunoglobulin G deficiency (disorder)"
          },
          {
            "code": "234550008",
            "display": "Immunoglobulin G1 deficiency (disorder)"
          },
          {
            "code": "234546001",
            "display": "Immunoglobulin G2 deficiency (disorder)"
          },
          {
            "code": "234548000",
            "display": "Immunoglobulin G3 deficiency (disorder)"
          },
          {
            "code": "234549008",
            "display": "Immunoglobulin G4 deficiency (disorder)"
          },
          {
            "code": "234539005",
            "display": "Immunoglobulin heavy chain deficiency (disorder)"
          },
          {
            "code": "234565009",
            "display": "Immunoglobulin hypercatabolism (disorder)"
          },
          {
            "code": "234543009",
            "display": "Immunoglobulin light chain deficiency (disorder)"
          },
          {
            "code": "234544003",
            "display": "Immunoglobulin subclass deficiency (disorder)"
          },
          {
            "code": "234553005",
            "display": "Immunoglobulin-associated molecule deficiency (disorder)"
          },
          {
            "code": "7990002",
            "display": "Immunoglobulinemia with isolated somatotropin deficiency (disorder)"
          },
          {
            "code": "254067002",
            "display": "Immuno-osseous dysplasia (disorder)"
          },
          {
            "code": "449853003",
            "display": "Interleukin-12 deficiency (disorder)"
          },
          {
            "code": "78378009",
            "display": "Isoimmune neutropenia (disorder)"
          },
          {
            "code": "764858009",
            "display": "Isolated agammaglobulinemia (disorder)"
          },
          {
            "code": "50926003",
            "display": "Job's syndrome (disorder)"
          },
          {
            "code": "449187006",
            "display": "Kappa light chain deficiency (disorder)"
          },
          {
            "code": "770942003",
            "display": "Kostmann syndrome (disorder)"
          },
          {
            "code": "449384005",
            "display": "Lambda light chain deficiency (disorder)"
          },
          {
            "code": "724179008",
            "display": "Laron syndrome with immunodeficiency (disorder)"
          },
          {
            "code": "71436005",
            "display": "Lazy leukocyte syndrome (disorder)"
          },
          {
            "code": "234582006",
            "display": "Leukocyte adhesion deficiency - type 1 (disorder)"
          },
          {
            "code": "234583001",
            "display": "Leukocyte adhesion deficiency - type 2 (disorder)"
          },
          {
            "code": "234586009",
            "display": "Leukocyte glucose-6-phosphate dehydrogenase deficiency (disorder)"
          },
          {
            "code": "763668009",
            "display": "Lichtenstein syndrome (disorder)"
          },
          {
            "code": "724177005",
            "display": "Ligase 4 syndrome (disorder)"
          },
          {
            "code": "234577004",
            "display": "Lipochrome histiocytosis - familial (disorder)"
          },
          {
            "code": "721977007",
            "display": "Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome (disorder)"
          },
          {
            "code": "191018006",
            "display": "Lymphocyte function antigen-1 defect (disorder)"
          },
          {
            "code": "25109007",
            "display": "Lymphopenic agammaglobulinemia - short-limbed dwarfism syndrome (disorder)"
          },
          {
            "code": "771073006",
            "display": "Lymphoproliferative disorder caused by methotrexate (disorder)"
          },
          {
            "code": "430478003",
            "display": "Macrophage activation syndrome (disorder)"
          },
          {
            "code": "191001007",
            "display": "Major histocompatibility complex class I deficiency (disorder)"
          },
          {
            "code": "191002000",
            "display": "Major histocompatibility complex class II deficiency (disorder)"
          },
          {
            "code": "234579001",
            "display": "Mannan-binding protein deficiency (disorder)"
          },
          {
            "code": "703538003",
            "display": "Mannose-binding lectin deficiency (disorder)"
          },
          {
            "code": "80255009",
            "display": "Maternal transfer neutropenia (disorder)"
          },
          {
            "code": "768560008",
            "display": "Melanoma differentiation-associated gene 5 deficiency (disorder)"
          },
          {
            "code": "718230004",
            "display": "Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency (disorder)"
          },
          {
            "code": "721876004",
            "display": "Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 2 deficiency (disorder)"
          },
          {
            "code": "723384004",
            "display": "Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency (disorder)"
          },
          {
            "code": "716869006",
            "display": "Mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency (disorder)"
          },
          {
            "code": "721877008",
            "display": "Mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency (disorder)"
          },
          {
            "code": "723385003",
            "display": "Mendelian susceptibility to mycobacterial disease due to partial interferon regulatory factor 8 deficiency (disorder)"
          },
          {
            "code": "723386002",
            "display": "Mendelian susceptibility to mycobacterial disease due to partial signal transducer and activator of transcription 1 deficiency (disorder)"
          },
          {
            "code": "234424007",
            "display": "Metabolic neutropenia (disorder)"
          },
          {
            "code": "304576008",
            "display": "Metaphyseal chondrodysplasia, McKusick type with associated immunodeficiency (disorder)"
          },
          {
            "code": "721903007",
            "display": "Microcephaly, hypogammaglobulinemia, abnormal immunity syndrome (disorder)"
          },
          {
            "code": "234638009",
            "display": "Microcephaly, normal intelligence and immunodeficiency (disorder)"
          },
          {
            "code": "778024005",
            "display": "Monocytopenia with susceptibility to infections (disorder)"
          },
          {
            "code": "234636008",
            "display": "Monosomy 22 and absence of immunoglobulin A (disorder)"
          },
          {
            "code": "24974008",
            "display": "Myelokathexis (disorder)"
          },
          {
            "code": "234433009",
            "display": "Myeloperoxidase deficiency (disorder)"
          },
          {
            "code": "737307003",
            "display": "Natural-killer cell deficiency (disorder)"
          },
          {
            "code": "773662009",
            "display": "Neonatal inflammatory skin and bowel disease (disorder)"
          },
          {
            "code": "416729007",
            "display": "Neutropenia associated with AIDS (disorder)"
          },
          {
            "code": "111585004",
            "display": "Neutropenia associated with autoimmune disease (disorder)"
          },
          {
            "code": "46359005",
            "display": "Neutropenia associated with infectious disease (disorder)"
          },
          {
            "code": "767658000",
            "display": "Neutropenia due to and following chemotherapy (disorder)"
          },
          {
            "code": "267540007",
            "display": "Neutropenia due to irradiation (disorder)"
          },
          {
            "code": "276576000",
            "display": "Neutropenia of the small for gestational age baby (disorder)"
          },
          {
            "code": "41814009",
            "display": "Neutropenia with dysgranulopoiesis (disorder)"
          },
          {
            "code": "725137007",
            "display": "Neutropenia, monocytopenia, deafness syndrome (disorder)"
          },
          {
            "code": "303011007",
            "display": "Neutropenic disorder (disorder)"
          },
          {
            "code": "723443003",
            "display": "Neutrophil immunodeficiency syndrome (disorder)"
          },
          {
            "code": "234587000",
            "display": "Neutrophil lactoferrin deficiency (disorder)"
          },
          {
            "code": "234588005",
            "display": "Neutrophil secondary granule deficiency (disorder)"
          },
          {
            "code": "414850009",
            "display": "Neutrophilia (disorder)"
          },
          {
            "code": "71610005",
            "display": "Neutrophilic leukemoid reaction (disorder)"
          },
          {
            "code": "55602000",
            "display": "Nezelof's syndrome (disorder)"
          },
          {
            "code": "3902000",
            "display": "Non dose-related drug-induced neutropenia (disorder)"
          },
          {
            "code": "773730002",
            "display": "Osteopetrosis hypogammaglobulinemia syndrome (disorder)"
          },
          {
            "code": "709608008",
            "display": "Periodontitis co-occurrent with acquired neutropenia (disorder)"
          },
          {
            "code": "709465004",
            "display": "Periodontitis co-occurrent with Ch+¬diak-Higashi syndrome (disorder)"
          },
          {
            "code": "710927004",
            "display": "Periodontitis co-occurrent with cyclical neutropenia (disorder)"
          },
          {
            "code": "710926008",
            "display": "Periodontitis co-occurrent with familial neutropenia (disorder)"
          },
          {
            "code": "709535007",
            "display": "Periodontitis co-occurrent with infantile genetic agranulocytosis (disorder)"
          },
          {
            "code": "710735009",
            "display": "Periodontitis co-occurrent with leukocyte adhesion deficiency (disorder)"
          },
          {
            "code": "234573000",
            "display": "Phagocytic cell defect (disorder)"
          },
          {
            "code": "302874002",
            "display": "Phagocytic cell dysfunction (disorder)"
          },
          {
            "code": "707152007",
            "display": "Phagocytic immunodeficiency (disorder)"
          },
          {
            "code": "773646003",
            "display": "Phospholipase C gamma 2 associated antibody deficiency and immune dysregulation (disorder)"
          },
          {
            "code": "772126000",
            "display": "Poikiloderma with neutropenia (disorder)"
          },
          {
            "code": "778027003",
            "display": "Primary CD59 deficiency (disorder)"
          },
          {
            "code": "58606001",
            "display": "Primary immune deficiency disorder (disorder)"
          },
          {
            "code": "718717004",
            "display": "Primary immunodeficiency syndrome due to p14 deficiency (disorder)"
          },
          {
            "code": "724275005",
            "display": "Primary immunodeficiency with natural killer cell deficiency and adrenal insufficiency (disorder)"
          },
          {
            "code": "234564008",
            "display": "Primary immunoglobulin catabolism abnormality (disorder)"
          },
          {
            "code": "191338000",
            "display": "Primary splenic neutropenia (disorder)"
          },
          {
            "code": "81166004",
            "display": "Properdin deficiency disease (disorder)"
          },
          {
            "code": "70349007",
            "display": "Pseudoneutrophilia (disorder)"
          },
          {
            "code": "60743005",
            "display": "Purine-nucleoside phosphorylase deficiency (disorder)"
          },
          {
            "code": "724015007",
            "display": "Pyogenic arthritis, pyoderma gangrenosum, acne syndrome (disorder)"
          },
          {
            "code": "718232007",
            "display": "Pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 (disorder)"
          },
          {
            "code": "105602005",
            "display": "Quantitative abnormality of granulocytes (disorder)"
          },
          {
            "code": "105601003",
            "display": "Quantitative disorder of neutrophils (disorder)"
          },
          {
            "code": "723508002",
            "display": "RAS-associated autoimmune leukoproliferative disease (disorder)"
          },
          {
            "code": "111584000",
            "display": "Reticular dysgenesis (disorder)"
          },
          {
            "code": "351287008",
            "display": "Reticular dysgenesis with congenital aleukocytosis (disorder)"
          },
          {
            "code": "773404000",
            "display": "Roifman syndrome (disorder)"
          },
          {
            "code": "723995003",
            "display": "Schimke immuno-osseous dysplasia (disorder)"
          },
          {
            "code": "36980009",
            "display": "SCID due to absent adenosine deaminase (disorder)"
          },
          {
            "code": "71904008",
            "display": "SCID due to absent class II HLA antigens (disorder)"
          },
          {
            "code": "111587007",
            "display": "SCID due to absent IL-2 receptor (disorder)"
          },
          {
            "code": "3439009",
            "display": "SCID due to absent peripheral T cell maturation (disorder)"
          },
          {
            "code": "49555001",
            "display": "SCID due to absent T cell receptor (disorder)"
          },
          {
            "code": "33286000",
            "display": "Secondary immune deficiency disorder (disorder)"
          },
          {
            "code": "234554004",
            "display": "Secretory piece deficiency (disorder)"
          },
          {
            "code": "190979003",
            "display": "Selective immunoglobulin A deficiency (disorder)"
          },
          {
            "code": "234541006",
            "display": "Selective immunoglobulin D deficiency (disorder)"
          },
          {
            "code": "234540007",
            "display": "Selective immunoglobulin E deficiency (disorder)"
          },
          {
            "code": "190981001",
            "display": "Selective immunoglobulin G deficiency (disorder)"
          },
          {
            "code": "234542004",
            "display": "Selective immunoglobulin M and immunoglobulin A deficiency (disorder)"
          },
          {
            "code": "190980000",
            "display": "Selective immunoglobulin M deficiency (disorder)"
          },
          {
            "code": "31323000",
            "display": "Severe combined immunodeficiency disease (disorder)"
          },
          {
            "code": "45390000",
            "display": "Severe combined immunodeficiency due to absent interleukin-2 production (disorder)"
          },
          {
            "code": "22406001",
            "display": "Severe combined immunodeficiency due to absent lymphoid stem cells (disorder)"
          },
          {
            "code": "771517009",
            "display": "Severe combined immunodeficiency due to caspase recruitment domain family member 11 deficiency (disorder)"
          },
          {
            "code": "765188009",
            "display": "Severe combined immunodeficiency due to complete recombination-activating gene 1 and/or recombination-activating gene 2 deficiency (disorder)"
          },
          {
            "code": "763623001",
            "display": "Severe combined immunodeficiency due to cytidine 5-prime triphosphate synthetase 1 deficiency (disorder)"
          },
          {
            "code": "715982006",
            "display": "Severe combined immunodeficiency due to deoxyribonucleic acid cross-link repair protein 1c deficiency (disorder)"
          },
          {
            "code": "716871006",
            "display": "Severe combined immunodeficiency due to deoxyribonucleic acid dependent protein kinase catalytic subunit deficiency (disorder)"
          },
          {
            "code": "718107000",
            "display": "Severe combined immunodeficiency T-cell negative B-cell positive due to janus kinase-3 deficiency (disorder)"
          },
          {
            "code": "722067005",
            "display": "Severe combined immunodeficiency with hypereosinophilia (disorder)"
          },
          {
            "code": "190998001",
            "display": "Severe combined immunodeficiency with low or normal B-cell numbers (disorder)"
          },
          {
            "code": "190997006",
            "display": "Severe combined immunodeficiency with low T- and B-cell numbers (disorder)"
          },
          {
            "code": "234570002",
            "display": "Severe combined immunodeficiency with maternofetal engraftment (disorder)"
          },
          {
            "code": "720853005",
            "display": "Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome (disorder)"
          },
          {
            "code": "190996002",
            "display": "Severe combined immunodefiency with reticular dysgenesis (disorder)"
          },
          {
            "code": "774211005",
            "display": "Severe dermatitis, multiple allergies, metabolic wasting syndrome (disorder)"
          },
          {
            "code": "720345008",
            "display": "Severe T-cell immunodeficiency, congenital alopecia, nail dystrophy syndrome (disorder)"
          },
          {
            "code": "89454001",
            "display": "Shwachman syndrome (disorder)"
          },
          {
            "code": "234556002",
            "display": "Specific antibody deficiency (disorder)"
          },
          {
            "code": "726078000",
            "display": "Sporadic Blau syndrome (disorder)"
          },
          {
            "code": "773702002",
            "display": "Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder)"
          },
          {
            "code": "127067009",
            "display": "Stress neutrophilia (finding)"
          },
          {
            "code": "766983005",
            "display": "Susceptibility to respiratory infection associated with CD8alpha chain mutation (disorder)"
          },
          {
            "code": "778045003",
            "display": "Susceptibility to viral and mycobacterial infection (disorder)"
          },
          {
            "code": "778023004",
            "display": "Syndromic multisystem autoimmune disease due to itchy E3 ubiquitin protein ligase deficiency (disorder)"
          },
          {
            "code": "765145001",
            "display": "T cell negative B cell positive severe combined immunodeficiency due to gamma chain deficiency (disorder)"
          },
          {
            "code": "770785002",
            "display": "T-cell immunodeficiency due to ras homolog family member H deficiency (disorder)"
          },
          {
            "code": "234608003",
            "display": "Terminal component deficiency (disorder)"
          },
          {
            "code": "190995003",
            "display": "Thymic aplasia or dysplasia with immunodeficiency (disorder)"
          },
          {
            "code": "402792003",
            "display": "T-lymphocyte immunodeficiency (disorder)"
          },
          {
            "code": "32092008",
            "display": "Toxic neutropenia (disorder)"
          },
          {
            "code": "88714009",
            "display": "Transient hypogammaglobulinemia of infancy (disorder)"
          },
          {
            "code": "234643002",
            "display": "Transient immunodeficiency of infancy (disorder)"
          },
          {
            "code": "55444004",
            "display": "Transient neonatal neutropenia (disorder)"
          },
          {
            "code": "234639001",
            "display": "Triple X syndrome, epilepsy, and hypogammaglobulinemia (disorder)"
          },
          {
            "code": "234584007",
            "display": "Tuftsin deficiency (disorder)"
          },
          {
            "code": "770687001",
            "display": "Vasculitis due to adenosine deaminase 2 deficiency (disorder)"
          },
          {
            "code": "719824001",
            "display": "Vici syndrome (disorder)"
          },
          {
            "code": "234571003",
            "display": "Warts, hypogammaglobulinemia, infections, and myelokathexis (disorder)"
          },
          {
            "code": "403837005",
            "display": "Wiskott-Aldrich autosomal dominant variant syndrome (disorder)"
          },
          {
            "code": "36070007",
            "display": "Wiskott-Aldrich syndrome (disorder)"
          },
          {
            "code": "65880007",
            "display": "X-linked agammaglobulinemia (disorder)"
          },
          {
            "code": "234533006",
            "display": "X-linked agammaglobulinemia with growth hormone deficiency (disorder)"
          },
          {
            "code": "403835002",
            "display": "X-linked hyper-immunoglobulin M syndrome (disorder)"
          },
          {
            "code": "234416002",
            "display": "X-linked hypogammaglobulinemia (disorder)"
          },
          {
            "code": "724276006",
            "display": "X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome (disorder)"
          },
          {
            "code": "719827008",
            "display": "X-linked immunoneurologic disorder (disorder)"
          },
          {
            "code": "719156006",
            "display": "X-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome (disorder)"
          },
          {
            "code": "77121009",
            "display": "X-linked lymphoproliferative syndrome (disorder)"
          },
          {
            "code": "719814009",
            "display": "X-linked mendelian susceptibility to mycobacterial disease (disorder)"
          },
          {
            "code": "718882006",
            "display": "X-linked severe congenital neutropenia (disorder)"
          }
        ]
      }
    ]
  }
}