Preferred Label : t(11;14);
NCIt definition : A cytogenetic abnormality that involves a translocation between chromosomes 11 and
14.;
NCI Metathesaurus CUI : CL509579;
Origin ID : C128641;
UMLS CUI : C4287831;
- Semantic type(s)
- concept_is_in_subset
- cytogenetic_abnormality_involves_chromosome