Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1136249
Disease: Mental Retardation, X-Linked
Mental Retardation, X-Linked
0.050 GeneticVariation disease BEFREE Most considerably, genotype-phenotype correlation studies of affected individuals in XLMR families with MRX gene mutations are necessary to define the criteria of MRX vs MRXS subclassification. 12485186 2002
CUI: C1136249
Disease: Mental Retardation, X-Linked
Mental Retardation, X-Linked
0.050 GeneticVariation disease BEFREE Here we report on the localization of a presumptive MRX gene to chromosomal region Xq24-q26 in a German family with nonspecific X-linked mental retardation (MRX 75, HUGO Human Gene Nomenclature Committee). 10946355 2000
CUI: C1136249
Disease: Mental Retardation, X-Linked
Mental Retardation, X-Linked
0.050 GeneticVariation disease BEFREE Thorough investigation of an MRX critical region in Xp22.1-21.3 enabled us to identify a new gene expressed in brain that is responsible for a non-specific form of X-linked mental retardation. 10471494 1999
CUI: C1136249
Disease: Mental Retardation, X-Linked
Mental Retardation, X-Linked
0.050 GeneticVariation disease BEFREE Further mutation analyses in males with X-linked mental retardation must prove that RSK4 is indeed a novel MRX gene. 10644430 1999
CUI: C1136249
Disease: Mental Retardation, X-Linked
Mental Retardation, X-Linked
0.050 GeneticVariation disease BEFREE MRX genes of 2 families with X-linked mental retardation (XLMR) were localized by linkage analysis. 8826456 1996