MeSH Browser

MeSH Supplementary: Chromosome 4q- Syndrome
Unique ID: C537639
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537639
Entry Term(s): Chromosome 4 Long Arm Deletion; Chromosome 4, monosomy 4q; Deletion 4q; Monosomy 4q
Registry Numbers: 0
Heading Mapped to: *Chromosome Deletion; Chromosomes, Human, Pair 4; *Chromosome Disorders
Frequency: 21
Note: A chromosomal abnormality characterized by loss of a portion of the long (Q) arm of chromosome 4. Severity of the syndrome depends on the size and location of the deletion and the genes that are lost. Affected individuals generally have distinct craniofacial features (FACIES), skeletal abnormalities, heart defects, intellectual disability, and short stature.
Date of Entry: 2010/08/25
Revision Date: 2016/09/29

Concept UI: M0535865
Terms: Monosomy 4q Preferred Term
Term UI T743259
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Chromosome 4, monosomy 4q
Term UI T743255
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Chromosome 4 Long Arm Deletion
Term UI T743256
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Deletion 4q
Term UI T743258
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010)

Chromosome 4q- Syndrome MeSH Supplementary Concept Data 2025