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immunodeficiency with hyper-IgM type 3

MIM.606843 20q12-q13.2

Wednesday 26 January 2011

This form of autosomal recessive hyper-IgM immunodeficiency (HIGM3) results from mutation in the CD40 gene (MIM.109535).

See also

- immunodeficiencies

  • constitutional immunodeficiencies (genetic immunodeficiencies)

- 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