t(1;17)(q42.3;q21.2)

Preferred Label : t(1;17)(q42.3;q21.2);

NCIt definition : A cytogenetic abnormality that refers to the translocation of chromosome 1q42.3 with chromosome 17q21.2. It results in the formation of IRF2BP2-RARA fusion gene. It is associated with the development of acute myeloid leukemia with t(1;17)(q42.3;q21.2); IRF2BP2-RARA.;

NCI Metathesaurus CUI : CL1906268;

Details

Origin ID

C198829;

cytogenetic_abnormality_involves_chromosome
- Human Chromosome 1 [NCIt concept]
- Human Chromosome 17 [NCIt concept]
is_abnormality_of_gene
- IRF2BP2/RARA Fusion Gene [NCIt concept]
is_cytogenetic_abnormality_of_disease
- Acute Myeloid Leukemia with t(1;17)(q42.3;q21.2); IRF2BP2-RARA [NCIt concept]
molecular_abnormality_involves_gene
- IRF2BP2 Gene [NCIt concept]
- IRF2BP2/RARA Fusion Gene [NCIt concept]
- RARA Gene [NCIt concept]

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