Chromosome Breakage

Preferred Label : Chromosome Breakage;

NCIt definition : A structural chromosomal abnormality caused by the spontaneous or induced breakage of a chromosome. It may result in DNA sequence deletions, chromosomal translocations, or chromosomal inversions.;

Détails

Origin ID

C85870;

UMLS CUI

C0376628;

Automatic exact mappings (from CISMeF team)
- Abnormality of chromosome stability [HPO term]
- Chromosome breakage [HRDO Sign]
- chromosome breakage [GO term]
Currated CISMeF NLP mapping
- Chromosome break (morphologic abnormality) [SNOMED CT concept]
- Chromosome breakage [HPO term]
- Chromosome breakage [LOINC component]
- chromosome break [Disease (Nov.)]
- chromosome break [SNOMED Notion]
- chromosome breakage [MeSH Descriptor]
- chromosome breakage [MeSH concept]
- chromosome breaks [MeSH concept]
Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
UMLS correspondences (same concept)
- Chromosome breakage [HPO term]
- Chromosome breakage [LOINC component]
- chromosome breakage [GO term]
- chromosome breakage [MeSH concept]
- chromosome breakage [MeSH Descriptor]

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

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