Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
0.120 Biomarker phenotype BEFREE MECP2-positive females had more problems in ambulation, muscle tone, tremor and ataxia, respiratory disturbances, head growth, hand use and stereotypies. 21982064 2012
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
0.120 GeneticVariation phenotype BEFREE Mutations in the methyl-CpG-binding protein 2 (MeCP2) cause Rett syndrome, a severe neurodevelopmental disease associated with ataxia and other post-natal symptoms similar to autism. 19319913 2009
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
0.120 CausalMutation phenotype CLINVAR