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
91 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Bruton-type agammaglobulinemia
(4)
Autosomal agammaglobulinemia
(1)
Agammaglobulinemia 2, autosomal recessive
(0)
Agammaglobulinemia 3, autosomal recessive
(0)
Agammaglobulinemia 4, autosomal recessive
(0)
Agammaglobulinemia 5, autosomal dominant
(0)
Agammaglobulinemia 6, autosomal recessive
(0)
Agammaglobulinemia 7, autosomal recessive
(0)
Agammaglobulinemia 8, autosomal dominant
(0)
Autosomal recessive agammaglobulinemia 1
(0)