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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 Common Variable Immune Deficiency primary antibody deficiency primary hypogammaglobulinemia secondary hypogammaglobulinemia idiopathic immunoglobulin deficiency common variable agammaglobulinemia sporadic hypogammaglobulinemia

This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C0009447 (MONDO:equivalentTo)
  • ICD9:279.06 (MONDO:i2s)
  • SCTID:23238000 (MONDO:equivalentTo)
  • NANDO:2200717 (https://orcid.org/0000-0003-0011-764X)
  • DOID:12177 (MONDO:equivalentTo)
  • NANDO:1200344 (https://orcid.org/0000-0003-0011-764X)
  • NCIT:C26725 (MONDO:equivalentTo)
  • icd11.foundation:1908371517 (MONDO:equivalentTo)
  • MESH:D017074 (Orphanet:1572/e)
  • MedDRA:10021449 (Orphanet:1572/e)
  • MEDGEN:40407 (MONDO:equivalentTo)
  • OMIMPS:607594 (https://orcid.org/0000-0002-6601-2165)
  • Orphanet:1572 (MONDO:equivalentTo)
  • GARD:6140 (MONDO:GARD)
  • NORD:990 (MONDO:NORD)
Subsets

gard_rare, ordo_disorder, matrix_llm__is_cancer_other, matrix_txgnn_grouping_cancer_or_benign_tumor, mondo_top_grouping_member, matrix_llm__txgnn_other, harrisons_view_immune_system_disorder, nord_rare, matrix_included, clingen, mondo_top_grouping_cancer_or_benign_tumor, matrix_txgnn_grouping_member, mondo_top_grouping_immune_system_disorder, rare, orphanet_rare, mondo_top_grouping_syndromic_disease, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, mondo_top_grouping_hematologic_disorder, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, susceptibility_mondo, matrix_llm__tag_existing_treatment_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_hematologic_disorder, harrisons_view_cancer_or_benign_tumor, harrisons_view_member, harrisons_view_syndromic_disease, harrisons_view_hereditary_disease

abbreviation
CVID [ Orphanet:1572 DOID:12177 ]

closeMatch

http://identifiers.org/meddra/10021449

curated content resource

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

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/mondo/sources/icd11foundation/1908371517

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

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

http://identifiers.org/medgen/40407

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

should conform to

http://purl.obolibrary.org/obo/mondo/patterns/OMIM_phenotypic_series.yaml

term tracker item

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