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: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:1240 | leukemia | A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. |
| DOID:9119 | acute myeloid leukemia | A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. |
| DOID:0060318 | acute promyelocytic leukemia | An acute myeloid leukemia characterized by accumulation of promyelocytes in the bone marrow and by a translocation between chromosomes 15 and 17. |
| DOID:8692 | myeloid leukemia | A leukemia that is located_in myeloid tissue. |
| DOID:0081081 | acute promyelocytic leukemia with PML-RARA | An acute promyelocytic leukemia that is characterized by a severe coagulopathy and the t(15;17)(q24;q21), generating a PML-RARA fusion gene, and where abnormal promyelocytes predominate. |
11 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:0060318 | DOID:0081081 |
| is_a | DOID:162 | DOID:0081081 |
| is_a | DOID:8692 | DOID:0081081 |
| is_a | DOID:2531 | DOID:0081081 |
| is_a | DOID:74 | DOID:0081081 |
| is_a | DOID:9119 | DOID:0081081 |
| is_a | DOID:0050686 | DOID:0081081 |
| is_a | DOID:14566 | DOID:0081081 |
| is_a | DOID:1240 | DOID:0081081 |
| is_a | DOID:7 | DOID:0081081 |
| is_a | DOID:4 | DOID:0081081 |
