t(10;19)(q26;q13)

Preferred Label : t(10;19)(q26;q13);

NCIt definition : A cytogenetic abnormality that refers to the translocation involving the genes CIC (capicua transcriptional suppressor) on chromosome 19 and DUX4L (double homeobox 4-like) on chromosome 10 resulting in CIC-DUX4L fusion.;

Détails

Origin ID

C120223;

UMLS CUI

C3897143;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- EWS Authorized Value Terminology [NCIt concept]
- EWS Molecular Analysis Table [NCIt concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 10 [NCIt concept]
- Human Chromosome 19 [NCIt concept]
is_abnormality_of_gene
- CIC/DUX4L Fusion Gene [NCIt concept]
- CIC/DUX4L10 Fusion Gene [NCIt concept]
is_cytogenetic_abnormality_of_disease
- CIC-DUX4L Sarcoma [NCIt concept]
molecular_abnormality_involves_gene
- CIC Gene [NCIt concept]
- CIC/DUX4L Fusion Gene [NCIt concept]

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

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