Immunodeficiency 39
ICD-10 Code
D84.8
Immunodeficiency 39
Definition
Any primary immunodeficiency disease in which the cause of the disease is a mutation in the IRF7 gene.
Also known as immunodeficiency 39, immunodeficiency type 39, IRF7 primary immunodeficiency disease, predisposition to severe viral infection due to IRF7 deficiency, primary immunodeficiency disease caused by mutation in IRF7 — per MONDO