Hyper-IgM syndrome type 5

Definition

Any hyper-IgM syndrome in which the cause of the disease is a mutation in the UNG gene.

Also known as HIGM5, hyper-IgM syndrome 5, hyper-IgM syndrome caused by mutation in UNG, hyper-IgM syndrome due to UNG deficiency, hyper-IgM syndrome due to uracil N-glycosylase, hyper-IgM syndrome type 5, immunodeficiency with hyper IgM, type 5, UNG hyper-IgM syndrome — per MONDO

Also identified as

• DOID 0060759 per MONDO
• OMIM 608106 per MONDO
• Orphanet 101092 per MONDO
• UMLS C1720958 per MONDO