FMR1, FMRP translational regulator 1, 2332

N. diseases: 346; N. variants: 10
Disease: Memory Loss ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0751295
Disease: Memory Loss
Memory Loss 		0.010 GeneticVariation phenotype BEFREE The purpose of this manuscript is to describe a series of adults with FMR1 alleles in the gray zone presenting with movement disorders or memory loss. 27372099 2016