Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8831
Gene Symbol: SYNGAP1
SYNGAP1
CUI: C1535926
Disease: Neurodevelopmental Disorders
Neurodevelopmental Disorders
0.330 Biomarker CTD_human De novo variants in neurodevelopmental disorders with epilepsy. 29942082

2018

Entrez Id: 8831
Gene Symbol: SYNGAP1
SYNGAP1
CUI: C1535926
Disease: Neurodevelopmental Disorders
Neurodevelopmental Disorders
0.330 Biomarker CTD_human Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases. 28191889

2017