Package | us.cdc.phinvads |
Resource Type | ValueSet |
Id | 2.16.840.1.114222.4.11.3060 |
FHIR Version | R4 |
Source | http://fhir.org/packages/us.cdc.phinvads |
URL | http://phinvads.cdc.gov/fhir/ValueSet/2.16.840.1.114222.4.11.3060 |
Version | 6 |
Status | active |
Date | 2019-01-15T00:04:00+11:00 |
Name | PHVS_ImmunosuppressedCondition_CDC |
Title | Immunosuppressed Condition |
Realm | us |
Description | Immunosuppressed conditions answer list based on SNOMED domain (234532001) |
No resources found
CodeSystem | |
sct | SNOMED CT (all versions) |
No narrative content found in resource
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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)" } ] } ] } }