Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.100 GeneticVariation group CLINVAR Exome sequencing in undiagnosed inherited and sporadic ataxias. 25497598 2015
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.100 GeneticVariation group CLINVAR Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism. 24267886 2013