t(7;16)(q33;p11)

Preferred Label : t(7;16)(q33;p11);

NCIt synonyms : t 7 16 q32-34 p11;

NCIt definition : A cytogenetic abnormality that refers to a chromosomal translocation involving the long arm (q33) of chromosome 7 and the short arm (p11) of chromosome 16. It is associated with the expression of FUS/CREB3L2 fusions and is a characteristic feature of low grade fibromyxoid sarcoma.;

Details

Origin ID

C45206;

UMLS CUI

C4053812;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 16 [NCIt concept]
- Human Chromosome 7 [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Childhood Low Grade Fibromyxoid Sarcoma [NCIt concept]
- Classical Low Grade Fibromyxoid Sarcoma [NCIt concept]
- Low Grade Fibromyxoid Sarcoma [NCIt concept]
- Low Grade Fibromyxoid Sarcoma with Giant Collagen Rosettes [NCIt concept]
molecular_abnormality_involves_gene
- CREB3L2 Gene [NCIt concept]
- FET Family Gene [NCIt concept]
- FUS Gene [NCIt concept]
- FUS/CREB3L2 Fusion Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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