oromandibular dystonia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A focal dystonia that is characterized by distortions of the mouth and tongue. (Human Disease Ontology, DOID_0050843)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012048
Similar Terms
Downloads & Tools

Genes

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

Symbol Name
ANO3 anoctamin 3
C19ORF12 chromosome 19 open reading frame 12
COASY CoA synthase
THAP1 THAP domain containing, apoptosis associated protein 1