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Acute myeloid leukemia (AML) with recurrent cytogenetic abnormalities
AML with characteristic molecular mutations: RUNX1, CEPA, NPM1, etc
AML, NOS/AML with dysplasia-related changes/therapy-related myeloid neoplasm
Myelodysplastic syndromes (MDS)
Chronic myelogenous leukemia (CML)
Polythesemia vera (PV)
Essential thrombocythemia (ET)
Primary myelofibrosis (PMF)
Mastocytosis
Myeloproliferative neoplasms (MPN), rare types (Chronic eosinophilic leukemia, Chronic neutrophilic leukemia)
Atypical CML
Chronic myelomonocytic leukemia (CMML)
Juvenile myelomonocytic leukemia (JMML)
Childhood MDS
Familial AML/MPN/MDS
Myeloid and lymphoid neoplasm with eosinophilia and abnormalities of PDGFRA, PDGFRB, or FGFR1. .
AML with characteristic molecular mutations: RUNX1, CEPA, NPM1, etc
AML, NOS/AML with dysplasia-related changes/therapy-related myeloid neoplasm
Myelodysplastic syndromes (MDS)
Chronic myelogenous leukemia (CML)
Polythesemia vera (PV)
Essential thrombocythemia (ET)
Primary myelofibrosis (PMF)
Mastocytosis
Myeloproliferative neoplasms (MPN), rare types (Chronic eosinophilic leukemia, Chronic neutrophilic leukemia)
Atypical CML
Chronic myelomonocytic leukemia (CMML)
Juvenile myelomonocytic leukemia (JMML)
Childhood MDS
Familial AML/MPN/MDS
Myeloid and lymphoid neoplasm with eosinophilia and abnormalities of PDGFRA, PDGFRB, or FGFR1. .