1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0111936 | immunodeficiency 14 | A combined T cell and B cell immunodeficiency characterized by B- and T-cell abnormalities and onset of recurrent sinopulmonary and other infections in early childhood that has_material_basis_in heterozygous activating mutation in the PIK3CD gene on chromosome 1p36.22. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:628 | combined T cell and B cell immunodeficiency | A primary immunodeficiency disease characterized by impaired T cell-mediated immunity and impaired B cell mediated humoral immunity. |
