Preferred Label : t(X;20)(p11.2;q13.3);
NCIt definition : A cytogenetic abnormality that refers to a chromosomal translocation that involves
the short arm (p11.2) of the X chromosome and the long arm (q13.3) of chromosome 20.;
NCI Metathesaurus CUI : CL1906506;
Origin ID : C199606;
UMLS CUI : C5855710;
Semantic type(s)
cytogenetic_abnormality_involves_chromosome