1 Child Term
Identifier | Name | Description |
---|---|---|
DOID:0110923 | familial hemophagocytic lymphohistiocytosis 3 | A hemophagocytic lymphohistiocytosis that has_material_basis_in a mutation of the UNC13D gene on chromosome 17q25.1. |
1 Parent Term
Identifier | Name | Description |
---|---|---|
DOID:2914 | immune system disease | A disease of anatomical entity that is located_in the immune system. |