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immunodeficiency with hyper-IgM type 2

MIM.605258 12p13

Wednesday 26 January 2011

This type 2 of autosomal recessive hyper-IgM immunodeficiency (HIGM2) results from mutation in the gene encoding activation-induced cytidine deaminase (AICDA; MIM.605257).

See also

- immunodeficiency with hyper-IgM