Common Variable Immunodeficiency

Preferred Label : Common Variable Immunodeficiency;

NCIt synonyms : Acquired Agammaglobulinemia; Secondary Hypogammaglobulinemia;

NCIt related terms : Common variable immune deficiency (CVID); Acquired Hypogammaglobulinemia;

NCIt definition : A primary immunodeficiency characterized by low levels or absence of all the immunoglobulin classes and lack of B-lymphocytes or plasma cells. It results in recurrent bacterial infections. Complications include autoimmune phenomena and cancer development.;

Alternative definition : NICHD: Abnormally low level of functional immunoglobulins in the blood that is not associated with a primary immunodeficiency.;

Détails

Origin ID

C26725;

UMLS CUI

C2936664;

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]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Acquired hypogammaglobulinaemia [MedDRA LLT]
- Acquired hypogammaglobulinemia [MedDRA LLT]
- hypogammaglobulinemia, acquired [MeSH concept]
associated_with_malfunction_of_gene_product
- Inducible T-Cell Costimulator [NCIt concept]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- GDC Terminology [NCIt concept]
- GDC Value Terminology [NCIt concept]
- NICHD Terminology [NCIt concept]
- Pediatric Adverse Events Terminology [NCIt concept]
- Pediatric Adverse Events Terminology Mapped to MedDRA [NCIt concept]
disease_has_associated_gene
- ICOS Gene [NCIt concept]
- ICOS wt Allele [NCIt concept]
disease_has_primary_anatomic_site
- Immune System [NCIt concept]
disease_may_have_associated_disease
- Lymphoproliferative Disease Associated with Primary Immune Disorder [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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