PSEN1, presenilin 1, 5663

N. diseases: 369; N. variants: 155
Disease: Developmental Academic Disorder ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1330966
Disease: Developmental Academic Disorder
Developmental Academic Disorder 		0.300 Biomarker phenotype CTD_human Notoginsenoside R1 increases neuronal excitability and ameliorates synaptic and memory dysfunction following amyloid elevation. 25213453 2014