A clonal hematopoietic disorder characterized by dysplasia and ineffective hematopoiesis in one or more of the hematopoietic cell lines. The dysplasia may be accompanied by an increase in myeloblasts, but the number is less than 20%, which, according to the WHO guidelines, is the requisite threshold for the diagnosis of acute myeloid leukemia. It may occur de novo or as a result of exposure to alkylating agents and/or radiotherapy. (WHO, 2001)
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Richter syndrome
MONDO:0002083
myelodysplastic syndrome with single lineage dysplasia
MONDO:0005272
myelodysplastic syndrome associated with isolated del(5q)
MONDO:0007925
Carney triad
MONDO:0011424
hereditary neoplastic syndrome
MONDO:0015356
myeloid/lymphoid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB, FGFR1 or JAK2
MONDO:0015688