common variable immunodeficiency

Preferred Label : common variable immunodeficiency;

MeSH definition : Heterogeneous group of immunodeficiency syndromes characterized by hypogammaglobulinemia of most isotypes, variable B-cell defects, and the presence of recurrent bacterial infections.;

MeSH synonym : common variable immunodeficiencies; immunodeficiency, common variable; immunodeficiencies, common variable; common variable hypogammaglobulinemia; common variable hypogammaglobulinemias; hypogammaglobulinemia, common variable; hypogammaglobulinemias, common variable; variable hypogammaglobulinemia, common; variable hypogammaglobulinemias, common; common variable immune deficiency;

MeSH hyponym : hypogammaglobulinemia, acquired; immunoglobulin deficiency, Late-Onset; Acquired Hypogammaglobulinemia; Acquired Hypogammaglobulinemias; Hypogammaglobulinemias, Acquired; Deficiencies, Late-Onset Immunoglobulin; Deficiency, Late-Onset Immunoglobulin; Immunoglobulin Deficiencies, Late-Onset; Immunoglobulin Deficiency, Late Onset; Late-Onset Immunoglobulin Deficiencies; Late-Onset Immunoglobulin Deficiency;

MeSH annotation : an immunodefic syndrome with hypogammaglobulinemia;

Wikipedia link : https://en.wikipedia.org/wiki/Acquired hypogammaglobulinemia;

Details

Origin ID

D017074;

UMLS CUI

C0009447;

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)
- Immunodeficiencies with severe reduction in at least two serum immunoglobulin isotypes with normal or low numbers of B cells [ICD-11 Sub-sub category]
- Other common variable immunodeficiencies [ICD-10 Sub-category (who)]
Currated CISMeF NLP mapping
- Acquired hypogammaglobulinaemia [MedDRA LLT]
- Acquired hypogammaglobulinemia [MedDRA LLT]
- Common Variable Immunodeficiency [NCIt concept]
- Common variable agammaglobulinemia (disorder) [SNOMED CT concept]
- Common variable immunodeficiency [ICD-10 category]
- Common variable immunodeficiency [PASCAL descriptor]
- Common variable immunodeficiency [ICD-11 More detail]
- Common variable immunodeficiency [ICD-9 code]
- Common variable immunodeficiency [ICD-10 category (who)]
- Common variable immunodeficiency [ORDO Disease]
- Common variable immunodeficiency [MedDRA LLT]
- Common variable immunodeficiency, unspecified [ICD-10 Sub-category (who)]
- Common variable immunodeficiency, unspecified [ICD-10 Sub-category]
- Immunodeficiency common variable [MedDRA Preferred Term]
- Immunodeficiency, common variable [OMIM phenotypic series]
- Immunodeficiency, common variable, 1 [OMIM Phenotype]
- Primary acquired hypogammaglobulinaemia [MedDRA LLT]
- Primary acquired hypogammaglobulinemia [MedDRA LLT]
- common variable agammaglobulinemia [SNOMED Notion]
- common variable immunodeficiency [Disease (Nov.)]
- common variable immunodeficiency [DO Concept]
DO Cross reference
- common variable immunodeficiency [DO Concept]
Manual BTNT mappings - CISMeF
- Common variable immunodeficiency due to TNFR deficiency [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Immunodeficiency predominantly affecting antibody production [ORDO Disease]
ORDO relation(s)
- Common variable immunodeficiency [ORDO Disease]
Record concept(s)
- common variable immunodeficiency [MeSH concept]
- hypogammaglobulinemia, acquired [MeSH concept]
- immunoglobulin deficiency, Late-Onset [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Common variable agammaglobulinemia (disorder) [SNOMED CT concept]
- Common variable immunodeficiency [ORDO Disease]
- Common variable immunodeficiency [MedDRA LLT]
- Common variable immunodeficiency [ICD-10 category]
- Common variable immunodeficiency [ICD-10 category (who)]
- Common variable immunodeficiency [ICD-9 code]
- Common variable immunodeficiency, unspecified [ICD-10 Sub-category]
- Immunodeficiency common variable [MedDRA Preferred Term]
- Primary acquired hypogammaglobulinaemia [MedDRA LLT]
- Primary acquired hypogammaglobulinemia [MedDRA LLT]
- common variable agammaglobulinemia [SNOMED Notion]
- common variable immunodeficiency [DO Concept]

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