t(3;3)(q21.3;q26.2)

Preferred Label : t(3;3)(q21.3;q26.2);

NCIt synonyms : t(3;3)(q21;q26.2); t 3 3 q21 q26 2; t(3;3)(q26;q21); t(3;3)(q21.3q26.2);

NCIt definition : A cytogenetic abnormality that refers to the translocation where both breakpoints are on the long arm (q23.1 and q26.2) of chromosome 3. It is associated with acute myeloid leukemia.;

Details

Origin ID

C36406;

UMLS CUI

C1515764;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- AML Authorized Value Terminology [NCIt concept]
- AML Minimal Residual Disease Table [NCIt concept]
- AML Molecular Analysis Table [NCIt concept]
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 3 [NCIt concept]
is_cytogenetic_abnormality_of_disease
- Acute Myeloid Leukemia with t(3;3) (q21.3;q26.2); GATA2, MECOM [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Acute Myeloid Leukemia Arising from Previous Myelodysplastic Syndrome [NCIt concept]
- Acute Myeloid Leukemia with Multilineage Dysplasia [NCIt concept]
- Recurrent Acute Myeloid Leukemia with Multilineage Dysplasia [NCIt concept]
- Recurrent Acute Myeloid Leukemia, Myelodysplasia-Related [NCIt concept]
molecular_abnormality_involves_gene
- GATA2 Gene [NCIt concept]
- GATA2/MECOM Fusion Gene [NCIt concept]
- MECOM Gene [NCIt concept]

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