SYT14, synaptotagmin 14, 255928

N. diseases: 34; N. variants: 8
Disease: Atrophic ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0333641
Disease: Atrophic
Atrophic 		0.010 GeneticVariation phenotype LHGDN Disruption of a synaptotagmin (SYT14) associated with neurodevelopmental abnormalities. 17304550 2007