isolated agammaglobulinemia
MONDO:0016462Also known as: isolated hypogammaglobulinemia, nonsyndromic agammaglobulinemia
- MONDO:
- MONDO:0016462
- Orphanet:
- 229717 ↗
Rare disease63 associated genes
Description
Isolated 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.
Associated genes
+53 more genes — install the extension to see the full list inline on any page.