t(10;11)(q21.3;q23.3)

Preferred Label : t(10;11)(q21.3;q23.3);

NCIt definition : A cytogenetic abnormality that refers to the translocation of the long arm (q21.3) of chromosome 10 and the long arm (q23.3) of chromosome 11 resulting in the formation of TET1/KMT2A fusion gene.;

NCI Metathesaurus CUI : CL1906304;

Details

Origin ID

C198867;

cytogenetic_abnormality_involves_chromosome
- Human Chromosome 10 [NCIt concept]
- Human Chromosome 11 [NCIt concept]
is_abnormality_of_gene
- KMT2A/TET1 Fusion Gene [NCIt concept]
is_cytogenetic_abnormality_of_disease
- Acute Myeloid Leukemia with t(10;11)(q21.3;q23.3); TET1-KMT2A [NCIt concept]
molecular_abnormality_involves_gene
- KMT2A Gene [NCIt concept]
- KMT2A/TET1 Fusion Gene [NCIt concept]
- TET1 Gene [NCIt concept]

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