MECP2, methyl-CpG binding protein 2, 4204

N. diseases: 90; N. variants: 362
Source: CURATED ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0424230
Disease: Motor retardation
Motor retardation
0.400 Biomarker phenotype CTD_human Phenotypic and genotypic variability in four males with MECP2 gene sequence aberrations including a novel deletion. 20098342 2010