Gene: CHD2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1106
Gene Symbol: CHD2
CHD2 		0.320 GeneticVariation disease BEFREE Only one CHD2 mutation was detected in patients with Lennox-Gastaut syndrome. 29314583 2018
Entrez Id: 1106
Gene Symbol: CHD2
CHD2 		0.320 GeneticVariation disease BEFREE Our findings suggest that CHD2 mutations are important in the etiological spectrum of LGS. 24614520 2014
Entrez Id: 1106
Gene Symbol: CHD2
CHD2 		0.320 GermlineCausalMutation disease ORPHANET Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1. 23708187 2013