Hyper-IgM syndrome
MONDO:0003947A 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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Browse by category →Sub-types of Hyper-IgM syndrome
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Hyper-IgM syndrome type 1 3 trials
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Hyper-IgM syndrome type 2 1 trial
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Hyper-IgM syndrome type 3 1 trial
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Hyper-IgM syndrome type 5 1 trial
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Hyper-IgM syndrome type 4 0 trials