Preferred Label : t(21;22);
NCIt definition : A cytogenetic abnormality that involves a translocation between chromosomes 21 and
22.;
NCI Metathesaurus CUI : CL509587;
Origin ID : C128644;
UMLS CUI : C4287942;
- Semantic type(s)
- concept_is_in_subset
- cytogenetic_abnormality_involves_chromosome