STX7, syntaxin 7, 8417

N. diseases: 14; N. variants: 5
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0266491
Disease: Neuronal heterotopia
Neuronal heterotopia
0.100 GeneticVariation disease CLINVAR Mosaic parental germline mutations causing recurrent forms of malformations of cortical development. 26395554 2016