Human genes for immunodeficiency 39
Immunodeficiency 39 [DOID:0111969]
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 IRF7 on chromosome 11p15.5.
Synonyms: immunodeficiency 39, DOID:0111969, IMD39