Disease: Mesial temporal sclerosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2062593
Disease: Mesial temporal sclerosis
Mesial temporal sclerosis 		0.020 GeneticVariation disease BEFREE Mesial Temporal Sclerosis in SCN1A-Related Epilepsy: Two Long-Term EEG Case Studies. 30117335 2019
CUI: C2062593
Disease: Mesial temporal sclerosis
Mesial temporal sclerosis 		0.020 GeneticVariation disease BEFREE We conclude that mesial temporal sclerosis is a common finding in children with SCN1A mutations. 22532537 2012