hypomimic face Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A reduced degree of motion of the muscles beneath the skin of the face, often associated with reduced facial crease formation. (Human Phenotype Ontology, HP_0000338)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000338
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Genes

2 genes associated with the hypomimic face phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATP1A3 ATPase, Na+/K+ transporting, alpha 3 polypeptide
CC2D1A coiled-coil and C2 domain containing 1A