folate-dependent fragile site at xq28 Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of a folate sensitive fragile site at chromosome Xq28. (Human Phenotype Ontology, HP_0003564)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003564
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Genes

1 genes associated with the folate-dependent fragile site at xq28 phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FMR1 fragile X mental retardation 1