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:2226 | myeloproliferative neoplasm | A myeloid neoplasm that is characterized by a group of slow growing blood cancers in which large numbers of abnormal red blood cells, white blood cells, or platelets grow and spread in the bone marrow and the peripheral blood. |
DOID:0111344 | myeloproliferative disorder with eosinophilia | A myeloproliferative neoplasm characterized by chronic proliferation of myeloid cells and eosinophilia in the peripheral blood and bone marrow that has_material_basis_in a fusion of the ETV6 and PDGFRB genes formed by a translocation from chromosome 12 to chromosome 5q32. |
11 Relations
Relationship |
Parent Term . Identifier |
Child Term . Identifier |
---|---|---|
is_a | DOID:2226 | DOID:0111344 |
is_a | DOID:4960 | DOID:0111344 |
is_a | DOID:74 | DOID:0111344 |
is_a | DOID:7 | DOID:0111344 |
is_a | DOID:4961 | DOID:0111344 |
is_a | DOID:2531 | DOID:0111344 |
is_a | DOID:4 | DOID:0111344 |
is_a | DOID:0070004 | DOID:0111344 |
is_a | DOID:14566 | DOID:0111344 |
is_a | DOID:162 | DOID:0111344 |
is_a | DOID:0050686 | DOID:0111344 |