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;
Origin ID : C199602;
UMLS CUI : C5855706;
Semantic type(s)
cytogenetic_abnormality_involves_chromosome
molecular_abnormality_involves_gene