FXR1, FMR1 autosomal homolog 1, 8087

N. diseases: 53; N. variants: 7
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability
0.020 GeneticVariation group BEFREE The Fragile X-Related 1 gene (FXR1) is a paralog of the Fragile X Mental Retardation 1 gene (FMR1), whose absence causes the Fragile X syndrome, the most common form of inherited intellectual disability. 23555284 2013
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability
0.020 GeneticVariation group BEFREE The Fragile X Mental retardation-Related 1 (FXR1) gene belongs to the fragile X related family, that also includes the Fragile X Mental Retardation (FMR1) gene involved in fragile X syndrome, the most common form of inherited mental retardation. 18628314 2008