STX1A, syntaxin 1A, 6804

N. diseases: 74; N. variants: 9
Disease: Facial Hemiatrophy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0015458
Disease: Facial Hemiatrophy
Facial Hemiatrophy 		0.010 Biomarker disease BEFREE Thus, we suggest a possible role of STX1A in the pathogenesis of HFA. 18593506 2008