| 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
FHIR{
"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)"
}
]
}
]
}
}