Agammaglobulinemia 1, autosomal recessive
A primary immunodeficiency characterized by profoundly low or absent serum antibodies and low or absent circulating B cells due to an early block of B-cell development. Affected individuals develop severe infections in the first years of life.
| Name | Development Level | Target Family |
|---|
| Name | Description |
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TCRDv4.6.9
UniProt Disease
UniProt Disease