Autosomal Agammaglobulinemia

Alias:
Agammaglobulinemia, Non-Bruton Type
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Autosomal Agammaglobulinemia, also known as agammaglobulinemia, non-bruton type, is related to agammaglobulinemia 9, autosomal recessive and agammaglobulinemia 10, autosomal dominant. An important gene associated with Autosomal Agammaglobulinemia is BLNK (B Cell Linker), and among its related pathways/superpathways are Prolactin Signaling and Phospholipase-C Pathway. Affiliated tissues include lung and skin, and related phenotypes are chronic otitis media and recurrent respiratory infections
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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9
142
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Medical Symptom

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Gene & Mutation

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Disease Model

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MGI
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References Literature

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