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
0.040 GeneticVariation disease BEFREE We also analyzed ACSL4 and DLG3, which have previously been known to cause XLMR and IL1RAPL2, a homologous gene for IL1RAPL1 that is mutated in autism and XLMR. 21384559 2011
CUI: C1136249
Disease: Mental Retardation, X-Linked
Mental Retardation, X-Linked
0.040 GeneticVariation disease BEFREE Mutations in ACSL4 are associated with non-syndromic X-linked mental retardation (MRX). 19617635 2009
CUI: C1136249
Disease: Mental Retardation, X-Linked
Mental Retardation, X-Linked
0.040 AlteredExpression disease LHGDN A third MRX family (MRX68) is the result of mutation in the long chain fatty acid-CoA ligase 4 (FACL4) gene: proposal of a rapid enzymatic assay for screening mentally retarded patients. 12525535 2003
CUI: C1136249
Disease: Mental Retardation, X-Linked
Mental Retardation, X-Linked
0.040 GeneticVariation disease BEFREE FACL4, encoding fatty acid-CoA ligase 4, is mutated in nonspecific X-linked mental retardation. 11889465 2002
CUI: C1136249
Disease: Mental Retardation, X-Linked
Mental Retardation, X-Linked
0.040 GeneticVariation disease LHGDN FACL4, encoding fatty acid-CoA ligase 4, is mutated in nonspecific X-linked mental retardation. 11889465 2002