12 Parents
| Identifier | Name | Description |
|---|---|---|
| DOID:0050686 | organ system cancer | A cancer that is classified based on the organ it starts in. |
| DOID:162 | cancer | A disease of cellular proliferation that is malignant and primary, characterized by uncontrolled cellular proliferation, local cell invasion and metastasis. |
| DOID:7 | disease of anatomical entity | A disease that manifests in a defined anatomical structure. |
| DOID:14566 | disease of cellular proliferation | A disease that is characterized by abnormally rapid cell division. |
| DOID:4 | disease | A disease is a disposition (i) to undergo pathological processes that (ii) exists in an organism because of one or more disorders in that organism. |
| DOID:4960 | bone marrow cancer | A hematopoietic cancer that derives_from the blood-forming stem cells of the bone marrow. |
| DOID:0070004 | myeloid neoplasm | A bone marrow cancer that is formed of any one of the bone marrow cells belonging to the granulocytic (neutrophil, eosinophil, basophil), monocytic/macrophage, erythroid, megakaryocytic and mast cell lineages. |
| DOID:4961 | bone marrow disease | A hematopoietic system disease that is located_in the bone marrow. |
| DOID:74 | hematopoietic system disease | A disease of anatomical entity that has_material_basis_in hematopoietic cells. |
| DOID:2531 | hematologic cancer | An organ system cancer located in the hematological system that is characterized by uncontrolled cellular proliferation in blood, bone marrow and lymph nodes. |
| DOID:0080164 | myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 | A myeloid neoplasm that is characterized by the formation of abnormal fusion genes that encode constitutively activated tyrosine kinases. |
| DOID:0080167 | myeloid and lymphoid neoplasms associated with FGFR1 abnormalities | A myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 that is characterized by the rearrangement of the FGFR1 gene, resulting in translocations with an 8p11 breakpoint. |
11 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:0080164 | DOID:0080167 |
| is_a | DOID:0050686 | DOID:0080167 |
| is_a | DOID:4 | DOID:0080167 |
| is_a | DOID:0070004 | DOID:0080167 |
| is_a | DOID:4961 | DOID:0080167 |
| is_a | DOID:2531 | DOID:0080167 |
| is_a | DOID:7 | DOID:0080167 |
| is_a | DOID:162 | DOID:0080167 |
| is_a | DOID:4960 | DOID:0080167 |
| is_a | DOID:14566 | DOID:0080167 |
| is_a | DOID:74 | DOID:0080167 |
