common variable immunodeficiency 7

Term ID

DOID:0081150

Synonyms

Definition

A common variable immunodeficiency that has_material_basis_in compound heterozygous mutation in the CD21 gene (CR2) on chromosome 1q32. https://pubmed.ncbi.nlm.nih.gov/22035880/

References

• OMIM:614699

Ontology

Human Disease   ( DOID:0081150 )