1 Child Term
Identifier | Name | Description |
---|---|---|
DOID:0051003 | congenital nonspherocytic hemolytic anemia 1 | A congenital nonspherocytic hemolytic anemia that has_material_basis_in mutation in the G6PD gene on chromosome Xq28, and is the most common genetic form of chronic and drug-, food-, or infection-induced hemolytic anemia. |
1 Parent Term
Identifier | Name | Description |
---|---|---|
DOID:720 | normocytic anemia | An anemia that is characterized by circulating red blood cells that are the same size and have a normal red color and a mean corpuscular volume (MCV) between 80 and 100 fL. |