Disease ID | Source | Name | Description |
618459 | OMIM | Immunodeficiency 62 (IMD62) | An autosomal recessive, primary immunologic disorder characterized by recurrent severe respiratory tract infections and bronchiectasis, due to antibody deficiency. Affected individuals have an abnormal B cell immunophenotype, with low levels of circulating memory B cells. The disease is caused by variants affecting the gene represented in this entry. |