MeSH Browser

MeSH Supplementary: Triple X syndrome
Unique ID: C535318
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535318
Entry Term(s): 47,XXX syndrome; 47,Xxx; Super female; Triple-X chromosome syndrome; Triple-X female; Triplo X syndrome; Trisomy X; XXX syndrome
Heading Mapped to: *Sex Chromosome Aberrations; *Trisomy; Chromosomes, Human, X; *Sex Chromosome Disorders of Sex Development
Frequency: 107
Note: A chromosomal abnormality characterized by the presence of an additional X chromosome in each of a female's cells. Affected individuals may be taller than average but they typically do not have any unusual physical features and most experience normal sexual development and are fertile. Triple X syndrome is associated with an increased risk of LEARNING DISORDERS and delayed development of speech and language skills. Delayed development of motor skills, HYPOTONIA, and behavioral and emotional disturbances may also occur. SEIZURES or kidney abnormalities occur in about 10 percent of cases.
Date of Entry: 2010/11/13
Revision Date: 2015/08/18

Concept UI: M0529779
Terms: Triple X syndrome Preferred Term
Term UI T735677
Date02/24/2009
LexicalTag NON
ThesaurusID; Trisomy X
Term UI T735676
Date02/24/2009
LexicalTag NON
ThesaurusID; Triple-X female
Term UI T735678
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Super female
Term UI T735679
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Triple-X chromosome syndrome
Term UI T735680
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); XXX syndrome
Term UI T735681
Date02/24/2009
LexicalTag NON
ThesaurusID; Triplo X syndrome
Term UI T735682
Date02/24/2009
LexicalTag NON
ThesaurusID; 47,XXX syndrome
Term UI T735675
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); 47,Xxx
Term UI T842610
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014)

Triple X syndrome MeSH Supplementary Concept Data 2024