1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0111989 | immunodeficiency 35 | A primary immunodeficiency disease characterized by increased susceptibility to mycobacterial infection after BCG vaccination and impaired cellular responses to IL-12, IFN-alpha/beta, IL-23, and IL-10 that has_material_basis_in homozygous or compound heterozygous mutation in the TYK2 gene on chromosome 19p13.2. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:2914 | immune system disease | A disease of anatomical entity that is located_in the immune system. |
