Search Ontology:
Human Disease

common variable immunodeficiency 4

Term ID
DOID:0081147
Synonyms
Definition
A common variable immunodeficiency that has_material_basis_in homozygous mutation in the BAFFR gene (TNFRSF13C), which encodes the B-cell activating factor receptor, on chromosome 22q13. https://pubmed.ncbi.nlm.nih.gov/19666484/
References
Ontology
Human Disease   ( DOID:0081147 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models