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Chromosome Fragility MeSH Descriptor Data 2023


MeSH Heading
Chromosome Fragility
Tree Number(s)
C23.550.210.110.180
C23.550.362.180.180
G05.365.590.175.165.180
G05.370.180.180
Unique ID
D002873
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D002873
Scope Note
Susceptibility of chromosomes to breakage leading to translocation; CHROMOSOME INVERSION; SEQUENCE DELETION; or other CHROMOSOME BREAKAGE related aberrations.
Entry Term(s)
Chromosomal Fragility
Previous Indexing
Chromosome Aberrations (1968-1981)
Chromosomes (1966-1967)
See Also
Chromosome Breakage
Chromosome Fragile Sites
Fragile X Syndrome
Trinucleotide Repeat Expansion
Public MeSH Note
82
History Note
82
Date Established
1982/01/01
Date of Entry
1981/02/23
Revision Date
2008/07/08
Chromosome Fragility Preferred
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