Chromosome 22 Loss of Heterozygosity

Preferred Label : Chromosome 22 Loss of Heterozygosity;

NCIt synonyms : Chromosome 22 LOH;

NCIt definition : A molecular abnormality that results in monoallelic loss of function mutations located within chromosome 22.;

NCI Metathesaurus CUI : CL937217;

Details

Origin ID

C157645;

UMLS CUI

C4763768;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
may_be_cytogenetic_abnormality_of_disease
- Type 2 Papillary Renal Cell Carcinoma [NCIt concept]

Keyword's position in hierarchy(ies) :

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