Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
0.120 GeneticVariation phenotype BEFREE These findings highlight the complexities of aberrant MECP2 function in Rett syndrome and explain some of the variation in manifestation of sleep disturbances. 27255190 2016
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
0.120 GeneticVariation phenotype BEFREE Seizures and sleep disturbances were more common than in those with MECP2 mutations whereas features of regression and spinal curvature were less common. 22872100 2013
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
0.120 Biomarker phenotype HPO