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- NCIT_C168760 IAO_0000115 "A cytogenetic abnormality that refers to the translocation of the long arm (q23) of chromosome 11 and the long arm (q12-21) of chromosome 19. It is associated with KMT2A (MLL) fusions, including those with MLLT6 (AF17), and acute myeloid leukemia." @default.
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- NCIT_C168760 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C168760 NCIT_P108 "t(11;17)(q23;q12-21)" @default.
- NCIT_C168760 NCIT_P208 "CL1378665" @default.
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- NCIT_C168760 hasExactSynonym "t(11;17)(q23;q12-21)" @default.
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