bruxism Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A sleep disorder that involves involuntarily grinding or clenching of the teeth while sleeping. (Human Disease Ontology, DOID_2846)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003763
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Genes

4 genes associated with the bruxism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FOXG1 forkhead box G1
MECP2 methyl CpG binding protein 2
PGAP3 post-GPI attachment to proteins 3
SHANK3 SH3 and multiple ankyrin repeat domains 3