Preferred Label : t(1;19);
NCIt definition : A cytogenetic abnormality that involves a translocation between chromosomes 1 and
19.;
NCI Metathesaurus CUI : CL509586;
Origin ID : C128654;
UMLS CUI : C4287943;
Semantic type(s)
concept_is_in_subset
cytogenetic_abnormality_involves_chromosome