1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0061007 | sideroblastic anemia 5 | A sideroblastic anemia that is characterized by abnormal iron accumulation in the mitochondria or erythroid cells that has_material_basis_in compound heterozygous mutation in the HSCB gene on chromosome 22q12. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:74 | hematopoietic system disease | A disease of anatomical entity that has_material_basis_in hematopoietic cells. |
