MeSH Browser

MeSH Supplementary: Fragile X Tremor Ataxia Syndrome
Unique ID: C564105
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564105
Entry Term(s): FXTAS Fragile X Tremor Ataxia Syndrome; Fragile X-Associated Tremor Ataxia Syndrome; Fxtas
Registry Numbers: 0
Heading Mapped to: *Ataxia; *Fragile X Syndrome; *Tremor
Frequency: 226
Note: An ataxia caused by expanded TRINUCLEOTIDE REPEATS in the FMR1 gene on the X chromosome. Occurs predominantly in men over 50 years of age. In addition to ataxia, TREMOR, brain atrophy, and DEMENTIA also occur. OMIM: 300623
Date of Entry: 2012/11/05
Revision Date: 2019/06/20

Concept UI: M0564405
Registry Numbers: 0
Terms: Fragile X Tremor Ataxia Syndrome Preferred Term
Term UI T829088
Date09/05/2012
LexicalTag NON
ThesaurusID; Fragile X-Associated Tremor Ataxia Syndrome
Term UI T000866576
Date09/15/2014
LexicalTag NON
ThesaurusID GHR (2014); FXTAS Fragile X Tremor Ataxia Syndrome
Term UI T000961640
Date06/20/2019
LexicalTag NON
ThesaurusID NLM (2019); Fxtas
Term UI T841450
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014)

Fragile X Tremor Ataxia Syndrome MeSH Supplementary Concept Data 2025