progeroid facial appearance Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A degree of wrinkling of the facial skin that is more than expected for the age of the individual, leading to a prematurely aged appearance. (Human Phenotype Ontology, HP_0005328)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005328
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Genes

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

Symbol Name
ERCC3 excision repair cross-complementation group 3
ERCC6 excision repair cross-complementation group 6
ERCC8 excision repair cross-complementation group 8
WRN Werner syndrome, RecQ helicase-like