Activation-induced cytidine deaminase deficiency (Q85056)

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This is a rare disease with the absence of immunoglobulin class switch recombination, the lack of immunoglobulin somatic hypermutations, and lymph node hyperplasia caused by the presence of giant germinal centres.
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ID_603312357
    English
    Activation-induced cytidine deaminase deficiency
    This is a rare disease with the absence of immunoglobulin class switch recombination, the lack of immunoglobulin somatic hypermutations, and lymph node hyperplasia caused by the presence of giant germinal centres.

      Statements

      CID11:ID_603312357
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      dki-india-ID_603312357
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      Concluído
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      13 August 2026
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