Monosomy 14 - CISMeF

Preferred Label : Monosomy 14;

NCIt definition : A chromosomal abnormality consisting of the absence of one of the copies of chromosome 14.;

NCI Metathesaurus CUI : CL359995;

Details

Origin ID

C185934;

UMLS CUI

C5670168;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 14 [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Diffuse Glioneuronal Tumor with Oligodendroglioma-Like Features and Nuclear Clusters [NCIt concept]

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