Term Name: common variable immunodeficiency 14
Synonyms:
Definition: A common variable immunodeficiency that has_material_basis_in heterozygous mutation in the IRF2BP2 gene on chromosome 1q42.
Ontology: Human Disease [DOID:0081156]   ( DOID:0081156 )

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