Gene: MECP2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4204
Gene Symbol: MECP2
MECP2 		0.500 Biomarker phenotype CTD_human Misregulation of the methyl-CpG-binding protein 2 (MECP2) gene has been found to cause a myriad of neurological disorders including autism, mental retardation, seizures, learning disabilities, and Rett syndrome. 19921286 2010
Entrez Id: 4204
Gene Symbol: MECP2
MECP2 		0.500 GeneticVariation phenotype LHGDN Early-onset encephalopathy and cortical myoclonus in a boy with MECP2 gene mutation. 15557528 2004
Entrez Id: 4204
Gene Symbol: MECP2
MECP2 		0.500 Biomarker phenotype HPO