Outbound Relationships |
Type |
Target |
Active |
Characteristic |
Refinability |
Group |
Values |
Acute myeloid leukemia, disease |
Is a |
Acute leukemia |
true |
Inferred relationship |
Some |
|
|
Acute myeloid leukemia, disease |
Is a |
Myeloid leukemia, disease (disorder) |
false |
Inferred relationship |
Some |
|
|
Acute myeloid leukemia, disease |
Finding site |
Bone marrow structure |
false |
Inferred relationship |
Some |
2 |
|
Acute myeloid leukemia, disease |
Course |
Acute |
false |
Inferred relationship |
Some |
|
|
Acute myeloid leukemia, disease |
Associated morphology |
Acute myeloid leukemia, no International Classification of Diseases for Oncology subtype |
false |
Inferred relationship |
Some |
3 |
|
Acute myeloid leukemia, disease |
Pathological process |
Malignant neoplastic process |
false |
Inferred relationship |
Some |
1 |
|
Acute myeloid leukemia, disease |
Associated morphology |
Myeloid leukemia - category |
false |
Inferred relationship |
Some |
4 |
|
Acute myeloid leukemia, disease |
Finding site |
Lymphoid system consists of lymph nodes, lymphatic vessels and organs that contain lymphoid tissue, e.g. thymus, spleen. |
false |
Inferred relationship |
Some |
1 |
|
Acute myeloid leukemia, disease |
Associated morphology |
Acute leukemia |
false |
Inferred relationship |
Some |
2 |
|
Acute myeloid leukemia, disease |
Associated morphology |
néoplasie maligne (morphologie) |
false |
Inferred relationship |
Some |
3 |
|
Acute myeloid leukemia, disease |
Finding site |
Bone marrow structure |
false |
Inferred relationship |
Some |
4 |
|
Acute myeloid leukemia, disease |
Finding site |
Bone marrow structure |
false |
Inferred relationship |
Some |
1 |
|
Acute myeloid leukemia, disease |
Finding site |
Hematopoietic system structure |
false |
Inferred relationship |
Some |
3 |
|
Acute myeloid leukemia, disease |
Finding site |
Bone marrow structure |
false |
Inferred relationship |
Some |
2 |
|
Acute myeloid leukemia, disease |
Finding site |
Bone marrow structure |
false |
Inferred relationship |
Some |
1 |
|
Acute myeloid leukemia, disease |
Is a |
Myeloid leukaemia |
true |
Inferred relationship |
Some |
|
|
Acute myeloid leukemia, disease |
Finding site |
Bone marrow structure |
false |
Inferred relationship |
Some |
2 |
|
Acute myeloid leukemia, disease |
Finding site |
Bone marrow structure |
false |
Inferred relationship |
Some |
3 |
|
Acute myeloid leukemia, disease |
Associated morphology |
néoplasie maligne (morphologie) |
false |
Inferred relationship |
Some |
1 |
|
Acute myeloid leukemia, disease |
Finding site |
Hematopoietic system structure |
false |
Inferred relationship |
Some |
1 |
|
Acute myeloid leukemia, disease |
Finding site |
Bone marrow structure |
false |
Inferred relationship |
Some |
1 |
|
Acute myeloid leukemia, disease |
Finding site |
Bone marrow structure |
false |
Inferred relationship |
Some |
2 |
|
Acute myeloid leukemia, disease |
Associated morphology |
Acute myeloid leukemia - category |
false |
Inferred relationship |
Some |
1 |
|
Acute myeloid leukemia, disease |
Finding site |
Bone marrow structure |
false |
Inferred relationship |
Some |
1 |
|
Acute myeloid leukemia, disease |
Finding site |
Bone marrow structure |
false |
Inferred relationship |
Some |
2 |
|
Acute myeloid leukemia, disease |
Finding site |
Bone marrow structure |
false |
Inferred relationship |
Some |
1 |
|
Acute myeloid leukemia, disease |
Finding site |
Bone marrow structure |
false |
Inferred relationship |
Some |
2 |
|
Acute myeloid leukemia, disease |
Finding site |
Bone marrow structure |
false |
Inferred relationship |
Some |
1 |
|
Acute myeloid leukemia, disease |
Finding site |
Bone marrow structure |
false |
Inferred relationship |
Some |
2 |
|
Acute myeloid leukemia, disease |
Associated morphology |
Acute myeloid leukemia - category |
false |
Inferred relationship |
Some |
1 |
|
Acute myeloid leukemia, disease |
Finding site |
Bone marrow structure |
true |
Inferred relationship |
Some |
1 |
|
Acute myeloid leukemia, disease |
Associated morphology |
Acute myeloid leukemia (morphologic abnormality) |
true |
Inferred relationship |
Some |
1 |
|
Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
A rare unclassified acute myeloid leukemia characterized by an acute panmyeloid proliferation with blasts constituting more than 20% of cells in the bone marrow or peripheral blood, accompanied by fibrosis of the bone marrow. Patients typically present with acute onset of severe constitutional symptoms, bone pain, and pancytopenia. Splenomegaly is minimal or absent. The disease is rapidly progressive with poor therapy response. |
Is a |
True |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Acute promyelocytic leukemia, FAB M3 |
Is a |
True |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Acute myelomonocytic leukemia, FAB M4 |
Is a |
True |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Acute myeloblastic leukemia |
Is a |
False |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
leucémie aigüe monoblastique |
Is a |
False |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Acute megakaryoblastic leukaemia |
Is a |
True |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Malignant myeloid/lymphoid neoplasm |
Is a |
False |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Acute myelogenous leukemia without differentiation, FAB M0 |
Is a |
False |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Acute myeloid leukaemia, minimal differentiation, FAB M0 |
Is a |
True |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Acute myelogenous leukemia without maturation, FAB M1 |
Is a |
False |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Acute myeloid leukemia without maturation, FAB M1 |
Is a |
True |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Acute myeloid leukemia with maturation, FAB M2 |
Is a |
True |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Acute monocytic leukemia, FAB M5 |
Is a |
False |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Acute myeloid leukemia in remission |
Is a |
True |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Acute megakaryoblastic leukemia, FAB M7 |
Is a |
False |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Granulocytic sarcoma |
Is a |
False |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Leukemic infiltration of skin in acute myeloid leukemia (disorder) |
Is a |
True |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Acute biphenotypic leukaemia |
Is a |
False |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
leucémie monocytaire/monoblastique aigue |
Is a |
False |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Basophilic leukemia |
Is a |
True |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Erythroleukemia, FAB M6 |
Is a |
True |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Myeloid sarcoma |
Is a |
False |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Acute myeloid leukemia with t(9:11)(p22;q23); MLLT3-MLL (disorder) |
Is a |
False |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Acute myeloid leukemia with myelodysplasia-related changes (disorder) |
Is a |
True |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Form of acute myeloid leukemia having a shortage of all types of mature blood cells with onset in childhood or young adulthood. |
Is a |
True |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Cytogenetically normal acute myeloid leukaemia |
Is a |
True |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
History of acute myeloid leukaemia |
Associated finding |
True |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
1 |
Therapy related acute myeloid leukemia and myelodysplastic syndrome (disorder) |
Is a |
False |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Akute myeloblastische Leukämie mit rekurrenter genetischer Anomalie |
Is a |
False |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Inherited acute myeloid leukemia (AML) is a rare, malignant hematologic disease characterized by clonal proliferation of myeloid blasts, primarily involving the bone marrow, in association with congenital disorders (e.g. Fanconi anemia, dyskeratosis congenita, Bloom syndrome, Down syndrome, congenital neutropenia, neurofibromatosis, etc.) and genetic defects predisposing to AML. Patients present with signs and symptoms related to ineffective hematopoesis (fatigue, bleeding and bruising, recurrent infections, bone pain) and/or extramedullary site involvement (gingivitis, splenomegaly, etc.). Depending on the underlying genetic defect, there may be additional cancer risks and other health problems present. |
Is a |
True |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Refractory acute myeloid leukaemia |
Is a |
True |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Relapsing acute myeloid leukemia (disorder) |
Is a |
True |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
A subtype of acute myeloid leukemia with recurrent genetic abnormalities characterized by leukocytosis, thrombocytosis and nonspecific symptoms related to ineffective hematopoiesis (fatigue, bleeding and bruising, recurrent infections, bone pain), with frequent extramedullary involvement typically presenting as gingival hyperplasia and lymphadenopathy. The disease is characterized by clonal proliferation of myeloid blasts harboring mutations of the NPM1 gene in the bone marrow, blood and other tissues. It is associated with multilineage dysplasia, involving the myeloid, monocytic, erythroid, and megakaryocytic cell lineages. |
Is a |
True |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13) is a rare subtype of acute myeloid leukemia with recurrent cytogenetic abnormalities characterized by clonal proliferation of myeloid blasts with predominantly megakaryoblastic differentiation in the bone marrow and blood, often with extensive infiltration of the abdominal organs. It occurs typically in infants and usually presents with hepatosplenomegaly, anemia, thrombocytopenia and nonspecific symptoms related to ineffective hematopoiesis (fatigue, bleeding and bruising, recurrent infections). Myelofibrosis and fibrosis of other infiltrated organs is also characteristic of this disease. |
Is a |
True |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
A subtype of acute myeloid leukaemia with recurrent genetic abnormalities, characterised by clonal proliferation of myeloid blasts harbouring somatic mutations of the CEBPA gene in the bone marrow, blood and, rarely, other tissues. It can present with anaemia, thrombocytopenia, and other nonspecific symptoms related to ineffective haematopoesis (fatigue, bleeding and bruising, recurrent infections, bone pain) and/or extramedullary site involvement (gingivitis, splenomegaly). |
Is a |
True |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
A distinct form of acute myeloid leukemia (AML) in which this chromosomal anomaly is found de novo or in therapy-related AML cases, and is characterized by frequent extramedullary involvement (mainly hepatomegaly, splenomegaly, lymphadenopathies, cutaneous infiltration, but also gum, bone, central nervous system, testicles involvement), severe coagulation disorder (disseminated intravascular coagulopathy or primary fibrinolysis) and poor prognosis. Morphologically, a blast population with a myelomonocytic stage of differentiation is observed. |
Is a |
True |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
A rare subtype of acute myeloid leukaemia with recurrent genetic abnormalities characterised by clonal proliferation of poorly differentiated myeloid blasts in the bone marrow, blood, or other tissues in patients who present the t(6;9)(p23;q34) translocation. Frequently associated with multilineage bone marrow dysplasia, it usually presents with anaemia, thrombocytopenia (often pancytopenia), and other nonspecific symptoms related to ineffective haematopoesis (fatigue, bleeding and bruising, recurrent infections, bone pain) and/or extramedullary site involvement (gingivitis, splenomegaly). Basophilia, as well as poor response to chemotherapy, has been reported. |
Is a |
True |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
A subtype of acute myeloid leukemia with recurrent genetic abnormalities characterized by clonal proliferation of myeloid blasts in the bone marrow, blood and, rarely, other tissues. Bone marrow typically shows small, hypolobated megakaryocytes and multilineage dysplasia. Patients typically present with leukocytosis, anemia, variable platelet counts and a variety of nonspecific symptoms related to ineffective hematopoesis (fatigue, bleeding, bruising, recurrent infections, bone pain) and/or extramedullary site involvement (gingivitis, splenomegaly). High resistance to conventional chemotherapy is reported. |
Is a |
True |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Acute myeloid leukemia with t(8;21)(q22;q22) RUNX1-RUNX1T1 (disorder) |
Is a |
True |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
A rare tumor arising from hematopoietic and lymphoid tissues characterized by abnormal proliferation and differentiation of a clonal population of myeloid stem cells carrying unspecific 11q23 abnormalities. Clinical manifestations result from accumulation of malignant myeloid cells within the bone marrow, peripheral blood and other organs, and include leukocytosis, anemia, thrombocytopenia, fatigue, anorexia and weight loss. |
Is a |
True |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
A rare acute myeloid leukemia (AML) with recurrent genetic anomaly characterized by the presence of bone marrow and peripheral blood myeloblasts with features ranging from those of minimal differentiation to granulocytic maturation, demonstrating t(9;22)(q34.1;q11.2) or molecular genetic evidence of BCR-ABL1 fusion. Evidence of chronic myeloid leukemia (CML) is absent. Patients most commonly present with leukocytosis with blast predominance and variable anemia and thrombocytopenia. Splenomegaly is less frequent and peripheral blood basophilia lower than in patients with myeloid blast transformation of CML. The disease occurs primarily in adults, and response to traditional AML therapy or tyrosine kinase inhibitor therapy alone is typically poor. |
Is a |
True |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Acute myeloid leukemia with CBFB::MYH11 fusion (disorder) |
Is a |
True |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Acute monocytic leukemia |
Is a |
True |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|
Myeloid leukemia associated with Down syndrome (disorder) |
Is a |
True |
Acute myeloid leukemia, disease |
Inferred relationship |
Some |
|