immunologic deficiency syndromes

Preferred Label : immunologic deficiency syndromes;

MeSH definition : Syndromes in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral.;

MeSH synonym : immunologic deficiency syndrome; syndromes, immunologic deficiency; immunological deficiency syndrome; immunological deficiency syndromes; syndromes, immunological deficiency; deficiency syndromes, immunologic; deficiency syndrome, immunologic; deficiency syndrome, immunological; deficiency syndromes, immunological; syndrome, immunological deficiency; syndrome, immunologic deficiency;

MeSH hyponym : antibody deficiency syndrome; Deficiency Syndromes, Antibody; Antibody Deficiency Syndromes; Deficiency Syndrome, Antibody; Syndrome, Antibody Deficiency; Syndromes, Antibody Deficiency;

MeSH annotation : GEN or unspecified; for defic of specific immunoprotein, IMMUNOGLOBULINS or specific immunoglobulin, use specific with /defic; TN 223: definition & use; TN 225: differentiation from immunoglobulin defic; Manual 23.25.2; DF: IMMUNOL DEFIC SYNDROMES; general or unspecified; prefer specifics; for deficiency of specific immunoprotein index the immunoprotein with /defic;

Details

Origin ID

D007153;

UMLS CUI

C0021051;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Deficiency of humoral immunity [ICD-9 code]
- Immune defect (finding) [SNOMED CT concept]
- Immunodeficiencies [Vue CIM-11]
- Immunodeficiency, unspecified [ICD-10 Sub-category (who)]
- Other immunodeficiencies [ICD-10 category (who)]
DO Cross reference
- primary immunodeficiency disease [DO Concept]
HPO term
- Immunodeficiency [HPO term]
MeSH Descriptor(s) used for indexing
- antibodies [MeSH Descriptor]
Metaterm(s)
- internal medicine [CISMeF Metaterm]
Record concept(s)
- antibody deficiency syndrome [MeSH concept]
- immunologic deficiency syndromes [MeSH concept]
Related MeSH Supplementary Concept(s)
- Activated PI3K-delta Syndrome [MeSH Supplementary Concept]
- B-Cell immunodeficiency, distal limb anomalies, and urogenital malformations [MeSH Supplementary Concept]
- C9 deficiency [MeSH Supplementary Concept]
- C9 deficiency with dermatomyositis [MeSH Supplementary Concept]
- CD8 deficiency, familial [MeSH Supplementary Concept]
- Cd4+ lymphocyte deficiency [MeSH Supplementary Concept]
- IRAK4 deficiency [MeSH Supplementary Concept]
- Kappa-Chain deficiency [MeSH Supplementary Concept]
- Kotzot-Richter syndrome [MeSH Supplementary Concept]
- LIG4 syndrome [MeSH Supplementary Concept]
- MASP2 deficiency [MeSH Supplementary Concept]
- MYD88 deficiency [MeSH Supplementary Concept]
- NEMO mutation with immunodeficiency [MeSH Supplementary Concept]
- Roifman-Chitayat syndrome [MeSH Supplementary Concept]
- T cell immunodeficiency primary [MeSH Supplementary Concept]
- T-Cell OKT4 deficiency [MeSH Supplementary Concept]
- WHIM syndrome [MeSH Supplementary Concept]
- antibody deficiency due to defect in CD19 [MeSH Supplementary Concept]
- cartilage hair hypoplasia like syndrome [MeSH Supplementary Concept]
- cartilage-hair hypoplasia [MeSH Supplementary Concept]
- chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature [MeSH Supplementary Concept]
- combined immunodeficiency with autoimmunity and spondylometaphyseal dysplasia [MeSH Supplementary Concept]
- combined inflammatory and immunologic defect [MeSH Supplementary Concept]
- complement component 3 deficiency, autosomal recessive [MeSH Supplementary Concept]
- complement component 4, partial deficiency of [MeSH Supplementary Concept]
- complement component 4a deficiency [MeSH Supplementary Concept]
- complement component 5 deficiency [MeSH Supplementary Concept]
- complement component 6 deficiency [MeSH Supplementary Concept]
- complement component 7 deficiency [MeSH Supplementary Concept]
- complement component C1s deficiency [MeSH Supplementary Concept]
- complement factor D deficiency [MeSH Supplementary Concept]
- davenport donlan syndrome [MeSH Supplementary Concept]
- diarrhea, Glucose-Stimulated secretory, with common variable immunodeficiency [MeSH Supplementary Concept]
- ectodermal dysplasia, anhidrotic, with T-Cell immunodeficiency, autosomal dominant [MeSH Supplementary Concept]
- ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema [MeSH Supplementary Concept]
- ectodermal dysplasia, hypohidrotic, with immune deficiency [MeSH Supplementary Concept]
- endotoxin hyporesponsiveness [MeSH Supplementary Concept]
- enteropathy, familial, with villous edema and immunoglobulin G2 deficiency [MeSH Supplementary Concept]
- fanconi like syndrome [MeSH Supplementary Concept]
- griscelli syndrome type 2 [MeSH Supplementary Concept]
- hepatic venoocclusive disease with immunodeficiency [MeSH Supplementary Concept]
- hypoglobulinemia and absent B cells [MeSH Supplementary Concept]
- immune deficiency disease [MeSH Supplementary Concept]
- immune deficiency, familial variable [MeSH Supplementary Concept]
- immunodeficiency due to defect in CD3-Epsilon [MeSH Supplementary Concept]
- immunodeficiency due to defect in CD3-Gamma [MeSH Supplementary Concept]
- immunodeficiency due to defect in CD3-Zeta [MeSH Supplementary Concept]
- immunodeficiency due to defect in MAPBP-Interacting protein [MeSH Supplementary Concept]
- immunodeficiency syndrome, variable [MeSH Supplementary Concept]
- immunodeficiency with defective leukocyte and lymphocyte function and with response to Histamine-1 antagonist [MeSH Supplementary Concept]
- immunodeficiency without anhidrotic ectodermal dysplasia [MeSH Supplementary Concept]
- immunodeficiency, X-Linked, with deficiency of 115,000 dalton surface glycoprotein [MeSH Supplementary Concept]
- immunodeficiency, gonadal dysgenesis, and pulmonary fibrosis [MeSH Supplementary Concept]
- immunodeficiency, hypogammaglobulinemia, and reduced B cells [MeSH Supplementary Concept]
- immunodeficiency, partial combined, with absence of HLA determinants and Beta-2-Microglobulin from lymphocytes [MeSH Supplementary Concept]
- inosine phosphorylase deficiency, immune defect due to [MeSH Supplementary Concept]
- interleukin 2 receptor, alpha, deficiency of [MeSH Supplementary Concept]
- invasive pneumococcal disease, recurrent isolated, 2 [MeSH Supplementary Concept]
- lichtenstein syndrome [MeSH Supplementary Concept]
- lymphoblastic transformation, intrinsic defect in [MeSH Supplementary Concept]
- lymphoid system deterioration, progressive [MeSH Supplementary Concept]
- lymphokine deficiency [MeSH Supplementary Concept]
- lymphopenic hypergammaglobulinemia, antibody deficiency, autoimmune hemolytic anemia, and glomerulonephritis [MeSH Supplementary Concept]
- majeed syndrome [MeSH Supplementary Concept]
- myelodysplasia, immunodeficiency, facial dysmorphism, short stature, and psychomotor delay [MeSH Supplementary Concept]
- natural killer cell deficiency, familial isolated [MeSH Supplementary Concept]
- neutrophil immunodeficiency syndrome [MeSH Supplementary Concept]
- properdin deficiency, type II [MeSH Supplementary Concept]
- properdin deficiency, type III [MeSH Supplementary Concept]
- riddle syndrome [MeSH Supplementary Concept]
- roifman syndrome [MeSH Supplementary Concept]
- schimke immunoosseous dysplasia [MeSH Supplementary Concept]
- severe combined immunodeficiency, autosomal recessive, T Cell-Negative, B Cell-Negative, NK Cell-Positive [MeSH Supplementary Concept]
- splenic hypoplasia [MeSH Supplementary Concept]
- thumb agenesis, short stature, and immunodeficiency [MeSH Supplementary Concept]
- thymic aplasia [MeSH Supplementary Concept]
- tuftsin deficiency [MeSH Supplementary Concept]
See also
- immunocompromised host [MeSH Descriptor]
See also (suggested by CISMeF)
- antibodies [MeSH Descriptor]
See also inter- (CISMeF)
- Drug-induced immunodeficiency (disorder) [SNOMED CT concept]
- Have Immunodeficiency [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Immunodeficiency [HPO term]
- Immunodeficiency [MedDRA Preferred Term]
- Immunodeficiency [LOINC component]
- Immunodeficiency [NCIt concept]
- Immunodeficiency NOS [MedDRA LLT]
- Immunodeficiency Syndrome [NCIt concept]
- Immunodeficiency disorder (disorder) [SNOMED CT concept]
- Immunodeficiency syndromes [MedDRA High Level Group Term]
- Immunodeficiency, unspecified [ICD-10 Sub-category]
- Unspecified immunity deficiency [ICD-9 code]
- Unspecified immunity deficiency [MedDRA LLT]
- immunodeficiency disorder [Radlex concept]
- immunodeficiency, nos [SNOMED Notion]
- primary immunodeficiency disease [DO Concept]
Validated automatic mappings to BTNT
- antibody deficiency syndrome [Disease (Nov.)]
- primary immunodeficiency disease [DO Concept]

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