facial wrinkling Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Excessive wrinkling of the skin of the face. (Human Phenotype Ontology, HP_0009762)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009762
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2 genes associated with the facial wrinkling phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
MED12 mediator complex subunit 12
NAA10 N(alpha)-acetyltransferase 10, NatA catalytic subunit