From: Role of reactive oxygen species in myelodysplastic syndromes
 | Blasts | Cytogenetics | Mutations |
---|---|---|---|
MDS with defining genetic abnormalities | |||
 MDS-5q (MDS with low blasts and isolated 5q deletion) | < 5% BM and < 2% peripheral blood | 5q deletion alone, or with one other abnormality other than monosomy 7 or 7q deletion |  |
 MDS-SF3B1 (MDS with low blasts and SF3B1 mutation) | < 5% BM and < 2% peripheral blood | Absence of 5q deletion, monosomy 7, or complex karyotype | SF3B1 |
 MDS-biTP53 (MDS with biallelic TP53 inactivation) | < 20% BM and peripheral blood | Generally complex | Two or more TP53 mutations, or one mutation with evidence of TP53 copy number loss or copy neutral loss of heterozygosity |
MDS, morphologically defined | |||
 MDS-LB (MDS with low blasts) | < 5% BM and < 2% peripheral blood |  |  |
 MDS-h (hypoplastic MDS) |  |  |  |
 MDS-IB (MDS with increased blasts) |  |  |  |
 MDS-IB1 | 5–9% BM or 2–4% peripheral blood |  |  |
 MDS-IB2 | 10–19% BM or 5–19% peripheral blood or Auer rods |  |  |
 | 5–19% BM; 2–19% peripheral blood |  |  |