Autosomal agammaglobulinemia

MONDO:0011096

Agammaglobulinemia, 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

42 clinical trials for this condition and its sub-types, 1 tagged with Autosomal agammaglobulinemia itself.

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Where it sits in the disease tree

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↑ Isolated agammaglobulinemia (4)

Sub-types of Autosomal agammaglobulinemia

Agammaglobulinemia 2, autosomal recessive 0 trials
Agammaglobulinemia 3, autosomal recessive 0 trials
Agammaglobulinemia 4, autosomal recessive 0 trials
Agammaglobulinemia 5, autosomal dominant 0 trials
Agammaglobulinemia 6, autosomal recessive 0 trials
Agammaglobulinemia 7, autosomal recessive 0 trials
Agammaglobulinemia 8, autosomal dominant 0 trials
Autosomal recessive agammaglobulinemia 1 0 trials

Including sub-types (42) Tagged with Autosomal agammaglobulinemia (1)

Trials to join now! 1

Scientists probe hidden IgE variants to unlock allergy mysteries

Knowledge-focused Recruiting now

This study looks at different forms of IgE (a protein involved in allergic reactions) in healthy volunteers and people with conditions like severe allergies, chronic hives, mastocytosis, and immune deficiencies. Researchers aim to understand how these IgE variations relate to hea…

Sponsor: KU Leuven • Aim: Knowledge-focused

Last updated Jun 27, 2026 08:09 UTC

Autosomal agammaglobulinemia

Where it sits in the disease tree

Scientists probe hidden IgE variants to unlock allergy mysteries