MeSH Browser

MeSH Supplementary: 49,XXXXX syndrome
Unique ID: C535319
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535319
Entry Term(s): Chromosome X pentasomy; Chromosome XXXXX syndrome; Penta-X syndrome; Pentasomy X; Pentasomy X syndrome
Heading Mapped to: *Aneuploidy; *Sex Chromosome Aberrations; *Sex Chromosome Disorders; Chromosomes, Human, X
Frequency: 7
Date of Entry: 2010/06/25
Revision Date: 1955/01/01

Concept UI: M0529780
Terms: 49,XXXXX syndrome Preferred Term
Term UI T735683
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Chromosome XXXXX syndrome
Term UI T735685
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Penta-X syndrome
Term UI T735686
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Pentasomy X syndrome
Term UI T735687
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010)

49,XXXXX syndrome MeSH Supplementary Concept Data 2024