Monarch Disease Ontology entry MONDO_0014597 (immunodeficiency 39) is 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 type 39, predisposition to severe viral infection due to IRF7 deficiency, primary immunodeficiency disease caused by mutation in IRF7.