Immunodeficiency 39

Any primary immunodeficiency disease in which the cause of the disease is a mutation in the IRF7 gene.

Also known as: IRF7 primary immunodeficiency disease, immunodeficiency 39, immunodeficiency type 39, predisposition to severe viral infection due to IRF7 deficiency, primary immunodeficiency disease caused by mutation in IRF7, IMD39

41 clinical trials for this condition and its sub-types, 0 tagged with Immunodeficiency 39 itself.