Gene: MEF2C ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4208
Gene Symbol: MEF2C
MEF2C 		0.110 Biomarker disease BEFREE MEF2C-related epilepsy has been poorly described in the literature, despite a consistent MEF2C haploinsufficiency phenotype characterized by severe language impairment and motor delay (MIM# 613443). 30922778 2019
Entrez Id: 4208
Gene Symbol: MEF2C
MEF2C 		0.110 Biomarker disease HPO