Chromosome Arm 1p Loss of Heterozygosity

Preferred Label : Chromosome Arm 1p Loss of Heterozygosity;

NCIt synonyms : 1p LOH; 1p Loss of Heterozygosity;

NCIt definition : A molecular abnormality that results in monoallelic loss of function mutations located within the short arm of chromosome 1 (1p).;

NCI Metathesaurus CUI : CL937183;

Details

Origin ID

C157626;

UMLS CUI

C4763752;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 1 [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Type 2 Papillary Renal Cell Carcinoma [NCIt concept]

Keyword's position in hierarchy(ies) :

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