Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4152
Gene Symbol: MBD1
MBD1
CUI: C0035372
Disease: Rett Syndrome
Rett Syndrome 		0.020 Biomarker BEFREE Together with other reported cases with interstitial deletion of 18q, a possible contribution of haploinsufficiency in both MBD1 and MBD2 genes to a Rett syndrome-like phenotype was suggested, but further genetic studies on other cases are necessary to clarify the genotype-phenotype correlation. 19813260

2010
Entrez Id: 4152
Gene Symbol: MBD1
MBD1
CUI: C0035372
Disease: Rett Syndrome
Rett Syndrome 		0.020 AlteredExpression LHGDN Identification of MeCP2 mutations in a series of females with autistic disorder. 12770674

2003