MeSH Browser

MeSH Supplementary: Chromosome 6, monosomy 6q
Unique ID: C537807
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537807
Entry Term(s): Deletion 6q; Monosomy 6q
Registry Numbers: 0
Heading Mapped to: *Chromosome Deletion; Chromosomes, Human, Pair 6
Frequency: 17
Note: A chromosomal abnormality that occurs when there is a deletion of the long (Q) arm of chromosome 6. The severity of the condition depend on the size and location of the deletion and which genes are involved. Affected individuals may experience developmental delay, intellectual disability, and have distinctive facial features (FACIES).
Date of Entry: 2010/08/25
Revision Date: 2016/09/29

Chromosome 6, monosomy 6q MeSH Supplementary Concept Data 2025