1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:5813 | purine nucleoside phosphorylase deficiency | A combined T cell and B cell immunodeficiency that is a rare autosomal recessive metabolic disorder that has_material_basis_in mutation in the PNP gene and characterized mainly by decreased T-cell function. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:2914 | immune system disease | A disease of anatomical entity that is located_in the immune system. |
