Term Name: common variable immunodeficiency 10
Synonyms:
Definition: A common variable immunodeficiency that has_material_basis_in heterozygous mutation in the NFKB2 gene on chromosome 10q24.
Ontology: Human Disease [DOID:0081152]   ( DOID:0081152 )

Relationships
is a type of: autosomal dominant disease common variable immunodeficiency