Preferred Label : t(1;22);
NCIt definition : A cytogenetic abnormality that involves a translocation between chromosomes 1 and
22.;
NCI Metathesaurus CUI : CL1412945;
Origin ID : C175584;
UMLS CUI : C5446638;
Semantic type(s)
concept_is_in_subset
cytogenetic_abnormality_involves_chromosome