STX1B, syntaxin 1B, 112755

N. diseases: 58; N. variants: 17
Disease: Seizure, Febrile, Complex ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0751057
Disease: Seizure, Febrile, Complex
Seizure, Febrile, Complex 		0.300 Biomarker disease CTD_human Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes. 25362483 2014