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common variable immunodeficiency

Go to external page http://purl.obolibrary.org/obo/MONDO_0015517

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: CVID primary antibody deficiency primary hypogammaglobulinemia secondary hypogammaglobulinemia idiopathic immunoglobulin deficiency common variable agammaglobulinemia sporadic hypogammaglobulinemia common variable immunodeficiency

This is just here as a test because I lose it

Term information

database cross reference
  • Orphanet:1572 (MONDO:equivalentTo)
  • UMLS:C0009447 (Orphanet:1572/e)
  • GARD:6140 (Orphanet:1572)
  • DOID:12177 (MONDO:equivalentTo)
  • OMIMPS:607594 (MONDO:equivalentTo)
  • MESH:D017074 (Orphanet:1572/e)
  • SCTID:23238000 (MONDO:equivalentTo)
  • NORD:990 (MONDO:NORD)
  • NCIT:C26725 (MONDO:equivalentTo)
  • ICD9:279.06 (MONDO:i2s)
  • MedDRA:10021449 (Orphanet:1572/e)
Subsets

gard_rare, ordo_disease, rare, nord_rare, orphanet_rare, clingen

IAO 0000233

https://github.com/monarch-initiative/mondo/issues/5507

closeMatch

http://identifiers.org/meddra/10021449

exactMatch

http://identifiers.org/snomedct/23238000

http://purl.obolibrary.org/obo/DOID_12177

http://linkedlifedata.com/resource/umls/id/C0009447

http://purl.obolibrary.org/obo/NCIT_C26725

http://www.orpha.net/ORDO/Orphanet_1572

https://omim.org/phenotypicSeries/PS607594

http://identifiers.org/mesh/D017074

has related synonym

Immunoglobulin deficiency, late-onset

common variable hypogamma-globulinemia

acquired hypogammaglobulinemia

common variable immune deficiency

acquired agammaglobulinemia

hypogamma-globulinemia, acquired

id

MONDO:0015517

seeAlso

https://search.clinicalgenome.org/kb/conditions/MONDO:0015517