Preferred Label : t(16;16);
NCIt definition : A cytogenetic abnormality that involves a translocation occurring within chromosome
16.;
NCI Metathesaurus CUI : CL509584;
Origin ID : C128645;
UMLS CUI : C4287945;
- Semantic type(s)
- concept_is_in_subset
- cytogenetic_abnormality_involves_chromosome