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Chromosome 18 ring MeSH Supplementary Concept Data 2024


MeSH Supplementary
Chromosome 18 ring
Unique ID
C538304
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C538304
Entry Term(s)
Ring Chromosome 18
ring 18 chromosome syndrome
Heading Mapped to
Chromosomes, Human, Pair 18
*Ring Chromosomes
Frequency
25
Note
Ring chromosome 18 arises when breaks occur at both ends of the chromosome, forming a circular structure. Affected individuals may have MICROCEPHALY; HYPERTELORISM; intellectual disability, and speech impairment. The severity of the disorders depends on how much genetic material is lost from the breaks.
Date of Entry
2010/08/25
Revision Date
2019/06/24
Chromosome 18 ring Preferred
ring 18 chromosome syndrome Related
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