SYP, synaptophysin, 6855

N. diseases: 243; N. variants: 3
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 Expression of VGLUTs contributes to degeneration and acquisition of learning and memory. 21295146 2011