Visualize Submit Comment

Metadata
ID	DOID:0081147
Name	common variable immunodeficiency 4
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/
Xrefs	MIM:613494
Parent Relationships	is_a common variable immunodeficiency
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance