Agammaglobulinemia 8a, Autosomal Dominant (AGM8A)

Alias:

Agammaglobulinemia, Autosomal Dominant, Due to Tcf3 Defect

Agammaglobulinemia 8, Autosomal Dominant

Agm8a

Agm8

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Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Agammaglobulinemia 8a, Autosomal Dominant, is also known as agammaglobulinemia, autosomal dominant, due to tcf3 defect. An important gene associated with Agammaglobulinemia 8a, Autosomal Dominant is TCF3 (Transcription Factor 3). Affiliated tissues include b cells and bone marrow, and related phenotypes are agammaglobulinemia and recurrent infections

Related ID：

MALACARDS：AGM027

OMIM：616941

MESH：D000361