Autosomal agammaglobulinemia
MONDO:0011096Agammaglobulinemia, non-Bruton type (autosomal agammaglobulinemia) is a rare form of agammaglobulinemia, a primary immunodeficiency disease, and is characterized by variable immune dysfunction with frequent and recurrent bacterial infections and/or chronic diarrhea.
Also known as: AGM, agammaglobulinemia, non-Bruton type, agammaglobulinemia, autosomal recessive, due to IGHM defect
89 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Agammaglobulinemia 2, autosomal recessive
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Agammaglobulinemia 3, autosomal recessive
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Agammaglobulinemia 4, autosomal recessive
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Agammaglobulinemia 5, autosomal dominant
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Agammaglobulinemia 6, autosomal recessive
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Agammaglobulinemia 7, autosomal recessive
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Agammaglobulinemia 8, autosomal dominant
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Autosomal recessive agammaglobulinemia 1
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