t(11;16)(p11;p11)

Preferred Label : t(11;16)(p11;p11);

NCIt definition : A cytogenetic abnormality that refers to the translocation of the short arm (p11) of chromosome 11 and the short arm (p11) of chromosome 16. It results in a FUS-CREB3L1 fusion.;

Détails

Origin ID

C121429;

UMLS CUI

C4053730;

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
- 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
- CREB3L1 Gene [NCIt concept]
- FET Family Gene [NCIt concept]
- FUS Gene [NCIt concept]
- FUS/CREB3L1 Fusion Gene [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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