Term Name: immunodeficiency 39
Synonyms: IMD39
Definition: A primary immunodeficiency disease characterized by impaired interferon I and III production in response to influenza virus infection that has_material_basis_in homozygous or compond heterozygous mutation in the IRF7 gene on chromosome 11p15.5.
Ontology: Human Disease [DOID:0111969]   ( DOID:0111969 )

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