Immunodeficiency 28

Definition

Any primary immunodeficiency disease in which the cause of the disease is a mutation in the IFNGR2 gene.

Also known as IFNGR2 primary immunodeficiency disease, immunodeficiency 28, immunodeficiency type 28, primary immunodeficiency disease caused by mutation in IFNGR2 — per MONDO

Also identified as

• DOID 0111995 per MONDO
• OMIM 614889 per MONDO
• UMLS C4013947 per MONDO