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 		0.110 GeneticVariation phenotype BEFREE Rett syndrome (RTT), a progressive neurological disorder mainly caused by mutations in MeCP2 gene, is commonly associated with gastrointestinal dysfunctions and constipation, suggesting a link between RTT's gastrointestinal abnormalities and the gut microbiota. 27473171 2016
Entrez Id: 4204
Gene Symbol: MECP2
MECP2 		0.110 Biomarker phenotype HPO