Preferred Label : t(12;13)(p13.2;q12.2);
NCIt definition : A cytogenetic abnormality that refers to the translocation of chromosome 12p13.2 with
chromosome 13q12.2. It results in ETV6-FLT3 fusion and is associated with myeloid/lymphoid
neoplasms with FLT3-rearrangement.;
NCI Metathesaurus CUI : CL1905742;
Origin ID : C198561;
- cytogenetic_abnormality_involves_chromosome
- may_be_cytogenetic_abnormality_of_disease
- molecular_abnormality_involves_gene