Search Ontology:
Human Disease

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
Ontology
Human Disease   ( DOID:0081150 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models