1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0111991 | immunodeficiency 62 | A B cell deficiency characterized by onset late in the first decade of life of recurrent upper and lower respiratory infections, impaired antibody response to vaccination, low levels of circulating memory B cells, and almost undetectable antibodies that has_material_basis_in homozygous or compound heterozygous mutation in the ARHGEF1 gene on chromosome 19q13.2. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:2914 | immune system disease | A disease of anatomical entity that is located_in the immune system. |
