Isolated agammaglobulinemia
MONDO:0016462Isolated agammaglobulinemia (IA) is the non-syndromic form of agammaglobulinemia, a primary immunodeficiency disease, and is characterized by deficient gamma globulins and associated predisposition to frequent and recurrent infections from infancy.
Also known as: isolated hypogammaglobulinemia, nonsyndromic agammaglobulinemia
45 clinical trials for this condition and its sub-types, 0 tagged with Isolated agammaglobulinemia itself.
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Sub-types of Isolated agammaglobulinemia
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Bruton-type agammaglobulinemia 4 trials
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Autosomal agammaglobulinemia 1 trial
8 sub-types
- 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
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