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Fragile X Tremor Ataxia Syndrome MeSH Supplementary Concept Data 2025


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
Fragile X Tremor Ataxia Syndrome Preferred
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