| Disease ID | Source | Name | Description |
| 617765 | OMIM | Immunodeficiency, common variable, 14 (CVID14) | A primary immunodeficiency resulting in recurrent sinopulmonary infections since early childhood, and characterized by hypogammaglobulinemia with undetectable IgG and IgA, poor response to vaccination, and decreased levels of switched memory B cells. CVID14 inheritance is autosomal dominant. The disease is caused by variants affecting the gene represented in this entry. |