Common variable immunodeficiency (CVID) comprises a heterogeneous group of diseases characterized by a significant hypogammaglobulinemia of unknown cause, failure to produce specific antibodies after immunizations and susceptibility to bacterial infections, predominantly caused by encapsulated bacteria. [ Orphanet:1572 ]
Synonyms: Common Variable Immune Deficiency CVID primary hypogammaglobulinemia primary antibody deficiency secondary hypogammaglobulinemia idiopathic immunoglobulin deficiency common variable agammaglobulinemia sporadic hypogammaglobulinemia
Term information
- MEDGEN:40407 (MONDO:equivalentTo)
- NANDO:2200717 (https://orcid.org/0000-0003-0011-764X)
- Orphanet:1572 (MONDO:equivalentTo)
- DOID:12177 (MONDO:equivalentTo)
- UMLS:C0009447 (MONDO:equivalentTo)
- MedDRA:10021449 (Orphanet:1572/e)
- MESH:D017074 (Orphanet:1572/e)
- OMIMPS:607594 (https://orcid.org/0000-0002-6601-2165)
- SCTID:23238000 (MONDO:equivalentTo)
- ICD9:279.06 (MONDO:i2s)
- NCIT:C26725 (MONDO:equivalentTo)
- NORD:990 (MONDO:NORD)
- GARD:6140 (MONDO:GARD)
- NANDO:1200344 (https://orcid.org/0000-0003-0011-764X)
ordo_disorder, gard_rare, otar, rare, nord_rare, orphanet_rare, clingen
http://identifiers.org/snomedct/23238000
http://purl.obolibrary.org/obo/DOID_12177
http://linkedlifedata.com/resource/umls/id/C0009447
http://www.orpha.net/ORDO/Orphanet_1572
http://purl.obolibrary.org/obo/NCIT_C26725
http://identifiers.org/medgen/40407
https://omim.org/phenotypicSeries/PS607594
http://identifiers.org/mesh/D017074
Immunoglobulin deficiency, late-onset
common variable hypogamma-globulinemia
acquired hypogammaglobulinemia
common variable immune deficiency
acquired agammaglobulinemia
hypogamma-globulinemia, acquired