| Disease Subtype(s) |
HCT Disease Inserts Required |
Cellular Therapy Disease Inserts Required |
AML with Defining Genetic Abnormalities
- Acute myeloid leukemia with MLLT3::KMT2A fusion (5)
- Acute myeloid leukemia with DEK::NUP214 fusion (6)
- Acute myeloid leukemia with MECOM, GATA2 rearrangement (7)
- Acute myeloid leukemia with RBM15::MRTFA fusion (8)
- Acute myeloid leukemia with other MECOM rearrangements (1011)
- Acute myeloid leukemia with RUNX1::RUNX1T1 fusion (281)
- Acute myeloid leukemia with CBFB::MYH11 fusion (282)
- Acute promyelocytic leukemia with PML::RARA fusion (283)
- Acute promyelocytic leukemia with other RARA fusions (1012)
- Acute myeloid leukemia with BCR::ABL1 fusion (3)
- Acute myeloid leukemia with NPM1 mutation (4)
- Acute myeloid leukemia with CEBPA mutation (297)
- Acute myeloid leukemia with other KMT2A rearrangements (284)
- AML with myelodysplasia – related changes (285)
- Acute myeloid leukemia with NUP98 rearrangement (1013)
- Acute myeloid leukemia with mutated TP53 (1014)
- Acute myeloid leukemia with other defined genetic alterations (1015)
Acute Myeloid Leukemia, Defined by Differentiation
- Acute myeloid leukemia with minimal differentiation (286)
- Acute myeloid leukemia without maturation (287)
- Acute myeloid leukemia with maturation (288)
- Acute myelomonocytic leukemia (289)
- Acute monocytic leukemia (290)
- Acute erythroid leukemia (291)
- Acute megakaryoblastic leukemia (292)
- Acute basophilic leukemia (293)
- Myeloid sarcoma (295)
|
Forms 2010 & 2110 |
No disease inserts required |
Last modified:
May 29, 2024
