Preferred Label : del(9p21-p22);
NCIt synonyms : del(9)(p21p22); del 9p21p22; del(9p21p22);
NCIt definition : A cytogenetic abnormality characterized by any loss of genetic material from the short
arm of chromosome 9 within the 9p21-p22 region.;
Origin ID : C36604;
UMLS CUI : C1515614;
Semantic type(s)
cytogenetic_abnormality_involves_chromosome
may_be_cytogenetic_abnormality_of_disease