STX1A:Ensemblv115

syntaxin 1A
OMIM: 186590, ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Green STX1A in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

2 reviews BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Literature
  • Expert Review Green
Phenotypes
  • neurodevelopmental disorder MONDO#0700092, STX1A-related