MeSH Browser

MeSH Supplementary: Chromosome 8, trisomy
Unique ID: C537942
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537942
Entry Term(s): Chromosome 8 duplication; Trisomy 8
Registry Number: 0
Heading Mapped to: Chromosomes, Human, Pair 8; *Trisomy
Frequency: 129
Note: A condition caused by an extra copy of chromosome 8. The effects can vary from normal development in some individuals, to facial, growth, and limb abnromalities, as well as delayed speech and intellectual disability. Trisomy 8 may also cause kidney, heart, and bone abnormalities.
Date of Entry: 2010/08/25
Revision Date: 2016/07/19

Chromosome 8, trisomy MeSH Supplementary Concept Data 2024