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- NCIT_C36371 IAO_0000115 "A cytogenetic abnormality that refers to the translocation of the long arm (q23.3) of chromosome 11 and the short arm (p13.1) of chromosome 19. It is associated with the development of acute myeloid leukemia with variant MLL translocations and topoisomerase II inhibitor-related acute myeloid leukemia." @default.
- NCIT_C36371 NCIT_A24 NCIT_C168895 @default.
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- NCIT_C36371 NCIT_A32 NCIT_C3420 @default.
- NCIT_C36371 NCIT_NHC0 "C36371" @default.
- NCIT_C36371 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C36371 NCIT_P108 "t(11;19)(q23.3;p13.1)" @default.
- NCIT_C36371 NCIT_P207 "C1515710" @default.
- NCIT_C36371 NCIT_P322 "GDC" @default.
- NCIT_C36371 NCIT_P322 "PCDC" @default.
- NCIT_C36371 NCIT_P366 "t_11_19_q23_p13_1" @default.
- NCIT_C36371 NCIT_P375 "t(11;19)(q23;p13.1)" @default.
- NCIT_C36371 NCIT_R173 NCIT_C12219 @default.
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- NCIT_C36371 NCIT_R173 NCIT_C14134 @default.
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- NCIT_C36371 NCIT_R177 NCIT_C21281 @default.
- NCIT_C36371 NCIT_R177 NCIT_C25870 @default.
- NCIT_C36371 NCIT_R177 NCIT_C26110 @default.
- NCIT_C36371 normalizedInformationContent "92.730304365937428" @default.
- NCIT_C36371 referenceCount "3" @default.
- NCIT_C36371 hasExactSynonym "t(11;19)(q23.3;p13.1)" @default.
- NCIT_C36371 hasExactSynonym "t(11;19)(q23;p13.1)" @default.
- NCIT_C36371 inSubset NCIT_C157711 @default.
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- NCIT_C36371 type Class @default.
- NCIT_C36371 isDefinedBy ncit.owl @default.
- NCIT_C36371 label "t(11;19)(q23.3;p13.1)" @default.
- NCIT_C36371 subClassOf B17476daf981e2908f5cd76bb7fccc126 @default.
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- NCIT_C36371 subClassOf NCIT_C36371 @default.
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- NCIT_C36371 subClassOf NCIT_C97926 @default.