Disease ID | Source | Name | Description |
608106 | OMIM | Immunodeficiency with hyper-IgM 5 (HIGM5) | A rare immunodeficiency syndrome characterized by normal or elevated serum IgM levels with absence of IgG, IgA, and IgE. It results in a profound susceptibility to bacterial infections. The disease is caused by variants affecting the gene represented in this entry. |