1 Child Term
Identifier | Name | Description |
---|---|---|
DOID:0081137 | agammaglobulinemia 3 | An agammaglobulinemia that has_material_basis_in homozygous mutation in the CD79A gene on chromosome 19q13.2. |
1 Parent Term
Identifier | Name | Description |
---|---|---|
DOID:630 | genetic disease | A disease that has_material_basis_in genetic variations in the human genome. |