9p21 Loss of Heterozygosity

Preferred Label : 9p21 Loss of Heterozygosity;

NCIt synonyms : 9p21 LOH;

NCIt definition : A molecular abnormality that results in monoallelic loss of function mutations located within 9p21.;

NCI Metathesaurus CUI : CL552237;

Details

Origin ID

C150431;

UMLS CUI

C4725726;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Disease Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]

Keyword's position in hierarchy(ies) :

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