MBD5, methyl-CpG binding domain protein 5, 55777

N. diseases: 120; N. variants: 31
Disease: Mental Retardation, Autosomal Dominant 1 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1969562
Disease: Mental Retardation, Autosomal Dominant 1
Mental Retardation, Autosomal Dominant 1 		0.610 Biomarker disease BEFREE Both MRD0+/MRD1+ and MRD0+/MRD1- patients had a significantly worse EFS (p = 0.0001) than those with undetectable MRD at both MRD0 and MRD1. 26449287 2017
CUI: C1969562
Disease: Mental Retardation, Autosomal Dominant 1
Mental Retardation, Autosomal Dominant 1 		0.610 GeneticVariation disease UNIPROT Disruption of an EHMT1-associated chromatin-modification module causes intellectual disability. 22726846 2012
CUI: C1969562
Disease: Mental Retardation, Autosomal Dominant 1
Mental Retardation, Autosomal Dominant 1 		0.610 GeneticVariation disease UNIPROT Copy-number variations measured by single-nucleotide-polymorphism oligonucleotide arrays in patients with mental retardation. 17847001 2007
CUI: C1969562
Disease: Mental Retardation, Autosomal Dominant 1
Mental Retardation, Autosomal Dominant 1 		0.610 Biomarker disease CTD_human
CUI: C1969562
Disease: Mental Retardation, Autosomal Dominant 1
Mental Retardation, Autosomal Dominant 1 		0.610 Biomarker disease GENOMICS_ENGLAND