Preferred Label : t(6;11);
NCIt definition : A cytogenetic abnormality that involves a translocation between chromosomes 6 and
11.;
NCI Metathesaurus CUI : CL509591;
Origin ID : C128651;
UMLS CUI : C4287937;
Semantic type(s)
concept_is_in_subset
cytogenetic_abnormality_involves_chromosome