common variable immunodeficiency 3

Term ID

DOID:0081146

Synonyms

Definition

A common variable immunodeficiency that has_material_basis_in homozygous or compound heterozygous mutation in the CD19 gene on chromosome 16p11.2. https://pubmed.ncbi.nlm.nih.gov/16672701/

References

• OMIM:613493

Ontology

Human Disease   ( DOID:0081146 )