MECP2, methyl-CpG binding protein 2, 4204

N. diseases: 664; N. variants: 387
Disease: Muscle hypotonia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.400 GeneticVariation phenotype CLINVAR Phenotypic manifestations of MECP2 mutations in classical and atypical Rett syndrome. 15057977 2004
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.400 CausalMutation phenotype CLINVAR Phenotypic manifestations of MECP2 mutations in classical and atypical Rett syndrome. 15057977 2004
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.400 GeneticVariation phenotype CLINVAR Neurodevelopmental disorders in males related to the gene causing Rett syndrome in females (MECP2). 12615169 2003
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.400 CausalMutation phenotype CLINVAR Neurodevelopmental disorders in males related to the gene causing Rett syndrome in females (MECP2). 12615169 2003
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.400 CausalMutation phenotype CLINVAR DNA recognition by the methyl-CpG binding domain of MeCP2. 11035019 2001
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.400 GeneticVariation phenotype CLINVAR Epilepsy in a representative series of Rett syndrome. 11227330 2001
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.400 CausalMutation phenotype CLINVAR Epilepsy in a representative series of Rett syndrome. 11227330 2001
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.400 GeneticVariation phenotype CLINVAR DNA recognition by the methyl-CpG binding domain of MeCP2. 11035019 2001
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.400 GeneticVariation phenotype CLINVAR Functional consequences of Rett syndrome mutations on human MeCP2. 11058114 2000
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.400 CausalMutation phenotype CLINVAR Functional consequences of Rett syndrome mutations on human MeCP2. 11058114 2000
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.400 GeneticVariation phenotype CLINVAR Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. 10508514 1999
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.400 CausalMutation phenotype CLINVAR Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. 10508514 1999
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.400 CausalMutation phenotype CLINVAR Dissection of the methyl-CpG binding domain from the chromosomal protein MeCP2. 8177735 1993
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.400 GeneticVariation phenotype CLINVAR Dissection of the methyl-CpG binding domain from the chromosomal protein MeCP2. 8177735 1993