Catalog
Hereditary agammaglobulinaemia with profoundly reduced or absent B cells
Link to WHO Definition
Hereditary agammaglobulinaemia with profoundly reduced or absent B cells – http://id.who.int/icd/entity/393046642
This refers to a hereditary type of primary immune deficiency disease characterised by a reduction in all types of gamma globulins, and rare X-linked genetic disorder that affects the body's ability to fight infection.