1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0111993 | immunodeficiency 55 | A combined immunodeficiency characterized by intrauterine growth retardation and a defect in DNA replication causing impaired immune cell differentiation in the bone marrow resulting in natural killer cell deficiency and chronic neutropenia that has_material_basis_in homozygous or compound heterozygous mutation in the GINS1 gene on chromosome 20p11.21. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:2914 | immune system disease | A disease of anatomical entity that is located_in the immune system. |
