1 Child Term
Identifier | Name | Description |
---|---|---|
DOID:0081152 | common variable immunodeficiency 10 | A common variable immunodeficiency that has_material_basis_in heterozygous mutation in the NFKB2 gene on chromosome 10q24. |
1 Parent Term
Identifier | Name | Description |
---|---|---|
DOID:2914 | immune system disease | A disease of anatomical entity that is located_in the immune system. |