Home > D. Systemic pathology > Immune system diseases > immunodeficiency with hyper-IgM type 2
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
- immunodeficiency with hyper-IgM type 1 / HIGM1 (MIM.308230) at Xq26
- immunodeficiency with hyper-IgM type 2 / HIGM2 (MIM.605258) at 12p13
- immunodeficiency with hyper-IgM type 3 / HIGM3 (MIM.606843) at 20q12-q13.2
- immunodeficiency with hyper-IgM type 4 / HIGM4 (MIM.608184)
- immunodeficiency with hyper-IgM type 5 / HIGM5 (MIM.608106) at 12q23-q24.1
