t(11;16)(q13;p13)

Preferred Label : t(11;16)(q13;p13);

NCIt definition : A cytogenetic abnormality that refers to the translocation involving the genes C11orf95 on chromosome 11 and MKL2 on chromosome 16 resulting in C11orf95-MKL2 fusion.;

Details

Origin ID

C121133;

UMLS CUI

C4053819;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 11 [NCIt concept]
- Human Chromosome 16 [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Chondroid Lipoma [NCIt concept]
molecular_abnormality_involves_gene
- MRTFB Gene [NCIt concept]
- ZFTA Gene [NCIt concept]
- ZFTA/MKL2 Fusion Gene [NCIt concept]

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