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Hyper-IgM syndrome

MONDO:0003947

A primary immune deficiency disorder characterized by defective CD40 signaling; via B cells affecting class switch recombination (CSR) and somatic hypermutation.

Also known as: immunodeficiency with hyper-IgM, hyperimmunoglobulin M syndrome

50 clinical trials for this condition and its sub-types, 8 tagged with Hyper-IgM syndrome itself.

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