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Bruton-type agammaglobulinemia

MONDO:0010421

X-linked agammaglobulinemia (XLA) is a clinically variable form of isolated agammaglobulinemia, an inherited immunodeficiency disorder, and is characterized in affected males by recurrent bacterial infections during infancy.

Also known as: BTK-deficiency, Bruton type agammaglobulinemia, Bruton's Sex-linked agammaglobulinemia, Bruton's X-linked agammaglobulinemia, Bruton-type agammaglobulinemia, X-linked agammaglobulinemia, agammaglobulinemia, X-linked 1, X-linked recessive, Bruton's agammaglobulinemia

45 clinical trials for this condition and its sub-types, 4 tagged with Bruton-type agammaglobulinemia itself.

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