Agammaglobulinemia 2, Autosomal Recessive (AGM2)

Alias:

Agammaglobulinemia 2

Agm2

Agammaglobulinemia, Autosomal Recessive, Due to Igll1 Defect

Agammaglobulinemia Autosomal Recessive Due to Igll1 Defect

Agammaglobulinemia, Type 2, Autosomal Recessive

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Medical Symptom

Gene & Mutation

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Disease Model

References Literature

Agammaglobulinemia 2, Autosomal Recessive, also known as agammaglobulinemia 2, is related to barth syndrome and agammaglobulinemia, x-linked. An important gene associated with Agammaglobulinemia 2, Autosomal Recessive is IGLL1 (Immunoglobulin Lambda Like Polypeptide 1). Affiliated tissues include b cells and t cells, and related phenotypes are recurrent otitis media and decreased circulating iga level

Related ID：

MALACARDS：AGM021

OMIM：613500

MESH：D000361