MeSH Browser

MeSH Supplementary: Chromosome 11q trisomy
Unique ID: C538297
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538297
Entry Term(s): Duplication 11q; Trisomy 11q
Registry Number: 0
Heading Mapped to: Chromosomes, Human, Pair 11; *Trisomy
Frequency: 14
Note: A chromosomal abnormality characterized by an extra copy or duplication of the long (Q) arm of chromosome 11. Severity of symptoms depend on the size and location of the duplication and which genes are involved. Affected individuals may experience developmental delay, psychomotor and intellectual disability, behavioral problems, and have distinct facial features (FACIES).
Date of Entry: 2010/08/25
Revision Date: 2016/09/29

Chromosome 11q trisomy MeSH Supplementary Concept Data 2023