Preferred Label : t(11;22);
NCIt definition : A cytogenetic abnormality that involves a translocation between chromosomes 11 and
22.;
NCI Metathesaurus CUI : CL509580;
Origin ID : C128642;
UMLS CUI : C4287949;
Semantic type(s)
concept_is_in_subset
cytogenetic_abnormality_involves_chromosome