Preferred Label : t(8;16);
NCIt definition : A cytogenetic abnormality that involves a translocation between chromosomes 8 and
16.;
NCI Metathesaurus CUI : CL1412944;
Origin ID : C175583;
UMLS CUI : C5446637;
Semantic type(s)
concept_is_in_subset
cytogenetic_abnormality_involves_chromosome