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
0.020 GeneticVariation disease BEFREE Moreover, loss of OCRL1 RhoGAP and the resulting alteration in Rho pathways may contribute to mental retardation in Lowe syndrome, as illustrated in other forms of X-linked mental retardation. 12915445 2003
CUI: C1136249
Disease: Mental Retardation, X-Linked
Mental Retardation, X-Linked
0.020 Biomarker disease BEFREE Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation. 9582072 1998