Preferred Label : Chromosome Arm 9p Loss of Heterozygosity;
NCIt synonyms : 9p LOH; 9p Loss of Heterozygosity;
NCIt definition : A molecular abnormality that results in monoallelic loss of function mutations located
within the short arm of chromosome 9 (9p).;
NCI Metathesaurus CUI : CL520604;
Origin ID : C132247;
UMLS CUI : C4331821;
- Semantic type(s)
- concept_is_in_subset
- may_be_cytogenetic_abnormality_of_disease