MeSH Browser

MeSH Supplementary: Chromosome Xq duplication syndrome
Unique ID: C536732
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536732
Entry Term(s): Chromosome Xq trisomy; Dup(Xq) syndrome; Duplication Xq; Trisomy Xq; X chromosome, trisomy Xq
Registry Numbers: 0
Heading Mapped to: *Sex Chromosome Aberrations; *Trisomy; *Sex Chromosome Disorders; Chromosomes, Human, X
Frequency: 6
Date of Entry: 2010/08/25
Revision Date: 1955/01/01

Concept UI: M0531193
Registry Numbers: 0
Terms: X chromosome, trisomy Xq Preferred Term
Term UI T740254
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Chromosome Xq trisomy
Term UI T740259
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Duplication Xq
Term UI T740256
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Trisomy Xq
Term UI T740255
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010)

Chromosome Xq duplication syndrome MeSH Supplementary Concept Data 2025