Preferred Label : t(1;13);
NCIt definition : A cytogenetic abnormality that involves a translocation between chromosomes 1 and
13.;
NCI Metathesaurus CUI : CL509585;
Origin ID : C128655;
UMLS CUI : C4287944;
- Semantic type(s)
- concept_is_in_subset
- cytogenetic_abnormality_involves_chromosome