Fragile X Tremor/ataxia Syndrome, also known as fragile x-associated tremor/ataxia syndrome,is related to fragile x-associated tremor/ataxia syndrome and ataxia,and has symptoms including cerebral cortical atrophy, incoordination and memory impairment. An important gene associated with Fragile X Tremor/ataxia Syndrome is FMR1 (Fragile X Mental Retardation 1). Affiliated tissues include cerebellum
Disease Interacts with Genes
Disease Interacts with Substances
Processes Associated With Trait
Molecular Function Associated With Trait
Biological Processes Associated With Trait
Symptoms Associated With Trait
Selected genes are highlighted in orange, bookmarked
genes are green
- Chemical increases gene,
- Chemical decreases gene,
- Chemical increases and decreases gene simultaneosly,
No arrows - gene doesn't interact with the chemical.
- Gene should be increased/decreased most of the time and the chemical does it.
- Gene should be increased/decreased most of the time but the chemical does the opposite.