facial myokymia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Facial myokymia is a fine fibrillary activity of one or more muscles innervated by the facial nerve (the seventh cranial nerve). (Human Phenotype Ontology, HP_0000317)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000317
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Genes

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

Symbol Name
ADCY5 adenylate cyclase 5
PPP2R2B protein phosphatase 2, regulatory subunit B, beta
PRKCG protein kinase C, gamma
SPTBN2 spectrin, beta, non-erythrocytic 2