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Autosomal agammaglobulinemia
rareAgammaglobulinemia, 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.
- Identifiers
- MONDO:0011096 Orphanet:33110
- Part of
- Isolated agammaglobulinemia
- Also known as
- agammaglobulinemia, non-Bruton type · AGM
Subtypes
Disease
- Agammaglobulinemia 2, autosomal recessive MONDO:0013287 IGLL1
- Agammaglobulinemia 3, autosomal recessive MONDO:0013288 CD79A
- Agammaglobulinemia 4, autosomal recessive MONDO:0013289 BLNK
- Agammaglobulinemia 5, autosomal dominant MONDO:0013290 LRRC8A
- Agammaglobulinemia 6, autosomal recessive MONDO:0012987 CD79B
- Agammaglobulinemia 7, autosomal recessive MONDO:0014083 PIK3R1
- Agammaglobulinemia 8, autosomal dominant MONDO:0014840 TCF3
- Autosomal recessive agammaglobulinemia 1 MONDO:0020729 IGHM
Projects
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