Term Name: immunodeficiency 132A
Synonyms: IMD132A
Definition: A primary immunodeficiency disease that is characterized by increased susceptibility to infection with certain pathogens and that has_material_basis_in heterozygous dominant-negative mutation in the TRAF3 gene on chromosome 14q32.
Ontology: Human Disease [DOID:0061101]   ( DOID:0061101 )

Relationships
is a type of: autosomal dominant disease primary immunodeficiency disease