" /> t(9;17)(q22;q11.2) - CISMeF





Preferred Label : t(9;17)(q22;q11.2);

NCIt definition : A cytogenetic abnormality that refers to a chromosomal translocation involving the long arm (q22) of chromosome 9 and the long arm (q11.2) of chromosome 17. It may be associated with the expression of TAF15/NR4A3 fusions and extraskeletal myxoid chondrosarcoma.;

NCI Metathesaurus CUI : CL1906509;

Details


You can consult :


Nous contacter.
03/05/2025


[Home] [Top]

© Rouen University Hospital. Any partial or total use of this material must mention the source.