del(3p25) - CISMeF

Preferred Label : del(3p25);

NCIt synonyms : del 3p25;

NCIt definition : A cytogenetic abnormality characterized by any loss of genetic material from the short arm of chromosome 3 within the band at 3p25.;

NCI Metathesaurus CUI : CL554686;

Détails

Origin ID

C41377;

UMLS CUI

C2931337;

Currated CISMeF NLP mapping
- Chromosome 3, monosomy 3p25 [MeSH concept]
- chromosome 3, monosomy 3p25 [MeSH Supplementary Concept]
Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
UMLS correspondences (same concept)
- Chromosome 3, monosomy 3p25 [MeSH concept]
- chromosome 3, monosomy 3p25 [MeSH Supplementary Concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 3 [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Pancreatic Serous Cystadenoma [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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