Hyper-IgM syndrome type 5

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

Also known as: HIGM5, UNG hyper-IgM syndrome, 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

42 clinical trials for this condition and its sub-types, 1 tagged with Hyper-IgM syndrome type 5 itself.